A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189694



Internal ID21328541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32397296..32397296hg38UCSC Ensembl
chr3:32438788..32438788hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3929042
Supporting Variants
SamplesHG002
Known GenesCMTM7
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189694
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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