A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15189234



Internal ID21328080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39247470..39247470hg38UCSC Ensembl
chr3:39288961..39288961hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933913
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15189234
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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