A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700356



Internal ID124022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23312204..23434145hg38UCSC Ensembl
chr15:23564854..23679292hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38121942
hg19114439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511734
Supporting Variants
Samples
Known GenesGOLGA8S, LOC440243
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700356
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.017801


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