A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702792



Internal ID126458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53052875..53052916hg38UCSC Ensembl
chr15:53345072..53345113hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541837
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702792
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004371


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