A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703955



Internal ID127621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69284874..69290874hg38UCSC Ensembl
chr15:69577213..69583213hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703955
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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