A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610183



Internal ID21802230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79274499..79279413hg38UCSC Ensembl
chr13:79848634..79853548hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg384915
hg194915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610183
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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