A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687321



Internal ID21209176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51709720..51709720hg38UCSC Ensembl
chr3:51743736..51743736hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg381477
hg191477
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807549
Supporting Variants
Samples
Known GenesGRM2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687321
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.666667


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