A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602062



Internal ID16042785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32009677..32020762hg38UCSC Ensembl
Innerchr6:31977454..31988539hg19UCSC Ensembl
Innerchr6:32085432..32096517hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3811086
hg1911086
hg1811086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10478n54
Supporting Variantsnssv1053801
Samples
Known GenesC4A, C4B, C4B_2, STK19, TNXA, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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