A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569142



Internal ID21761185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35826477..35826477hg38UCSC Ensembl
chr6:35794254..35794254hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068735
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569142
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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