A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977515



Internal ID22752450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33079804..33080593hg38UCSC Ensembl
chr6:33047581..33048370hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445466
Samples
Known GenesHLA-DPA1, HLA-DPB1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977515
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer