A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17540713



Internal ID21865068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112328688..112330749hg38UCSC Ensembl
chr3:112047535..112049596hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg382062
hg192062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17540713
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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