A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602060



Internal ID16042783
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 StatusM
Merged Variantsdgv10476n54
Supporting Variantsnssv1053797, nssv1053798, nssv1053799, nssv1053796
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)nsv602060
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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