A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047962



Internal ID99840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63549737..63585264hg38UCSC Ensembl
chr11:63317209..63352736hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3835528
hg1935528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510354
Supporting Variants
Samples
Known GenesHRASLS2, MIR3680-1, MIR3680-2, PLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047962
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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