A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602997



Internal ID16043720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:43221202..43291349hg38UCSC Ensembl
Innerchr6:43188940..43259087hg19UCSC Ensembl
Innerchr6:43296918..43367065hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3870148
hg1970148
hg1870148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058420
Samples
Known GenesCUL9, DNPH1, TTBK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602997
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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