A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682824



Internal ID21204680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52898370..52898489hg38UCSC Ensembl
chr3:52932386..52932505hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682824
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.65625


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