A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606641



Internal ID21798688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82769292..82769292hg38UCSC Ensembl
chr13:83343427..83343427hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606641
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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