I'm trying to analyse some RNA-seq data which was handed to me with very little info, only fastq files.

I first trimmed illumina adapters and then ran Hisat2 on the most recent GRCh38 primary assembly with:

hisat2-build Homo_sapiens.GRCh38.dna.primary_assembly.fa hg38
hisat2 -x hg38/hg38 -1 trimmed_${name1}_R1.fastq.gz -2 trimmed_${name1}_R2.fastq.gz -S ${name1}.sam

and I don't get particularly great alignment rate (only 50% or so). When I look at the bam files on IGV, there is only alignments on chr1, 10 and 11.

I've checked with idxstats:

 samtools idxstats ${name1}.nodup.srt.bam | head -n 10
1       248956422       10142469        148
10      133797422       4686247 103
11      26070428        2051017 13
*       0       0       15262866

and it confirms that only chr1, 10 and 11 are there. Why is Hisat2 only aligning to chromosomes with 1 in the name? Did I do something incorrect with the hisat2-build?

Thanks