A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556140



Internal ID21880495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71935113..71935113hg38UCSC Ensembl
chr3:71984264..71984264hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556140
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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