A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602005



Internal ID16042728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31984717..32021501hg38UCSC Ensembl
Innerchr6:31952494..31989278hg19UCSC Ensembl
Innerchr6:32060473..32097256hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3836785
hg1936785
hg1836784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10466n54
Supporting Variantsnssv1053639
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)nsv602005
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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