A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602026



Internal ID16042749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31986316..32038127hg38UCSC Ensembl
Innerchr6:31954093..32005904hg19UCSC Ensembl
Innerchr6:32062072..32113883hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3851812
hg1951812
hg1851812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10468n54
Supporting Variantsnssv1053711
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)nsv602026
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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