A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601981



Internal ID16042704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31983430..32035067hg38UCSC Ensembl
Innerchr6:31951207..32002844hg19UCSC Ensembl
Innerchr6:32059186..32110823hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3851638
hg1951638
hg1851638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10468n54
Supporting Variantsnssv1053581
Samples
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2, STK19, TNXA, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601981
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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