A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602057



Internal ID16042780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32005403..32038127hg38UCSC Ensembl
Innerchr6:31973180..32005904hg19UCSC Ensembl
Innerchr6:32081158..32113883hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3832725
hg1932725
hg1832726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10477n54
Supporting Variantsnssv1053793
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)nsv602057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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