A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189874



Internal ID21328697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133560768..133560768hg38UCSC Ensembl
chr3:133279612..133279612hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3947923
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189874
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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