A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702961



Internal ID126627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43718874..43728050hg38UCSC Ensembl
chr15:44011072..44020248hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg389177
hg199177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702961
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001418


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