A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726749



Internal ID19025030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13060017..13140112hg38UCSC Ensembl
Innerchr2:13200142..13280237hg19UCSC Ensembl
Innerchr2:13117593..13197688hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3880096
hg1980096
hg1880096
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008439
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726749
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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