A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186360



Internal ID21325178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35580687..35580687hg38UCSC Ensembl
chr20:34168609..34168609hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949933
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186360
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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