A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612692



Internal ID21804739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111517894..111518267hg38UCSC Ensembl
chr13:112170241..112170614hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028364
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612692
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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