A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053799



Internal ID15560299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32007072..32029276hg38UCSC Ensembl
Innerchr6:31974849..31997053hg19UCSC Ensembl
Innerchr6:32082827..32105046hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3822205
hg1922205
hg1822220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602060
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)nssv1053799
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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