A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030566



Internal ID19119785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170556631..170673434hg38UCSC Ensembl
Innerchr6:170865719..170982522hg19UCSC Ensembl
Innerchr6:170707644..170824447hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38116804
hg19116804
hg18116804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6209n100
Supporting Variantsnssv3653100
Samples
Known GenesPDCD2, TBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030566
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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