A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617297



Internal ID21809344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110813079..110813253hg38UCSC Ensembl
chr13:111465426..111465600hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617297
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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