A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524874



Internal ID18823155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:105542008..105817472hg38UCSC Ensembl
Innerchr12:105935786..106211250hg19UCSC Ensembl
Innerchr12:104459916..104735380hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38275465
hg19275465
hg18275465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039068
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)nssv3524874
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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