A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602033



Internal ID16042756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31988864..32038945hg38UCSC Ensembl
Innerchr6:31956641..32006722hg19UCSC Ensembl
Innerchr6:32064620..32114701hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3850082
hg1950082
hg1850082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10468n54
Supporting Variantsnssv1053724
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)nsv602033
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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