A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726762



Internal ID19025043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13062181..13139820hg38UCSC Ensembl
Innerchr2:13202306..13279945hg19UCSC Ensembl
Innerchr2:13119757..13197396hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3877640
hg1977640
hg1877640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012680
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)nssv3726762
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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