A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15178942



Internal ID21317738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32765254..32766569hg38UCSC Ensembl
chr3:32806746..32808061hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3941636
Supporting Variants
SamplesHG002
Known GenesCNOT10
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15178942
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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