A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733731



Internal ID19032012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75459391..75777023hg38UCSC Ensembl
Innerchr3:75508542..75826174hg19UCSC Ensembl
Innerchr3:75591232..75908864hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38317633
hg19317633
hg18317633
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012001
Supporting Variants
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3733731
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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