A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602917



Internal ID16043640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35496921..35497706hg38UCSC Ensembl
Innerchr6:35464698..35465483hg19UCSC Ensembl
Innerchr6:35572676..35573461hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38786
hg19786
hg18786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10625n54
Supporting Variantsnssv1058205
Samples
Known GenesTEAD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602917
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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