A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703370



Internal ID127036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96057119..96057175hg38UCSC Ensembl
chr15:96600348..96600404hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519572
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703370
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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