A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616258



Internal ID21808305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111545482..111545790hg38UCSC Ensembl
chr13:112197829..112198137hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616258
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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