A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699605



Internal ID123271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28462874..28602874hg38UCSC Ensembl
chr15:28708020..28848020hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38140001
hg19140001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146117
Supporting Variants
Samples
Known GenesGOLGA8F, GOLGA8G, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699605
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008562


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