A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053624



Internal ID15560124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31984645..32038826hg38UCSC Ensembl
Innerchr6:31952422..32006603hg19UCSC Ensembl
Innerchr6:32060401..32114582hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3854182
hg1954182
hg1854182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601998
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)nssv1053624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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