A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588966



Internal ID21781009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61974302..61974302hg38UCSC Ensembl
chr11:61741774..61741774hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096746
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588966
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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