A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610803



Internal ID21802850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78970620..78970620hg38UCSC Ensembl
chr13:79544755..79544755hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610803
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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