A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053794



Internal ID15560294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32005403..32042485hg38UCSC Ensembl
Innerchr6:31973180..32010262hg19UCSC Ensembl
Innerchr6:32081158..32118241hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3837083
hg1937083
hg1837084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602058
Supporting Variants
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)nssv1053794
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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