A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702964



Internal ID126630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43785357..43785980hg38UCSC Ensembl
chr15:44077555..44078178hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512583
Supporting Variants
Samples
Known GenesSERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702964
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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