A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998302



Internal ID18811152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32595752..33112754hg38UCSC Ensembl
Innerchr3:32637244..33154246hg19UCSC Ensembl
Innerchr3:32612248..33129250hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38517003
hg19517003
hg18517003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589586
Samples
Known GenesCCR4, CNOT10, GLB1, TMPPE, TRIM71
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998302
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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