A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701627



Internal ID125293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44818350..44827874hg38UCSC Ensembl
chr15:45110548..45120072hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg389525
hg199525
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517617
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701627
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.017157


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