A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619949



Internal ID21811996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39109684..39109684hg38UCSC Ensembl
chr20:37738327..37738327hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619949
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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