A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569297



Internal ID21761340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23394057..23394057hg38UCSC Ensembl
chr6:23394285..23394285hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079960
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569297
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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