A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603477



Internal ID16390886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65926311..66086775hg38UCSC Ensembl
Innerchr6:66636204..66796668hg19UCSC Ensembl
Innerchr6:66692925..66853389hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38160465
hg19160465
hg18160465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10733n54
Supporting Variantsnssv1062721
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603477
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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