A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190082



Internal ID21328928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72447090..72447090hg38UCSC Ensembl
chr3:72496241..72496241hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937160
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190082
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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