A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602012



Internal ID16389421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31985690..31993705hg38UCSC Ensembl
Innerchr6:31953467..31961482hg19UCSC Ensembl
Innerchr6:32061446..32069461hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg388016
hg198016
hg188016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10471n54
Supporting Variantsnssv1053656
Samples
Known GenesC4A, C4B, C4B_2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602012
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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