A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596995



Internal ID21789038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63461531..63461531hg38UCSC Ensembl
chr11:63229003..63229003hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg385917
hg195917
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085225
Supporting Variants
Samples
Known GenesHRASLS5, MIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596995
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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