A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702880



Internal ID126546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63820879..63820889hg38UCSC Ensembl
chr15:64113078..64113088hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3811
hg1911
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558033
Supporting Variants
Samples
Known GenesHERC1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702880
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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