A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699600



Internal ID123266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28390537..28570250hg38UCSC Ensembl
chr15:28635683..28815396hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38179714
hg19179714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145465
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)nssv17699600
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.080897


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