A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602038



Internal ID16042761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31993705..32006368hg38UCSC Ensembl
Innerchr6:31961482..31974145hg19UCSC Ensembl
Innerchr6:32069461..32082123hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812664
hg1912664
hg1812663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053729
Samples
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602038
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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