A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602085



Internal ID16042808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32018543..32027095hg38UCSC Ensembl
Innerchr6:31986320..31994872hg19UCSC Ensembl
Innerchr6:32094298..32102850hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg388553
hg198553
hg188553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10481n54
Supporting Variantsnssv1053867
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)nsv602085
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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