A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677964



Internal ID21199821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32765256..32766570hg38UCSC Ensembl
chr3:32806748..32808062hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381315
hg191315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808371
Supporting Variants
Samples
Known GenesCNOT10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677964
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.790323


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