A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179738



Internal ID21318534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39218864..39218930hg38UCSC Ensembl
chr3:39260355..39260421hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3943341
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179738
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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