A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602037



Internal ID16042760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31993089..32045574hg38UCSC Ensembl
Innerchr6:31960866..32013351hg19UCSC Ensembl
Innerchr6:32068845..32121329hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3852486
hg1952486
hg1852485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10468n54
Supporting Variantsnssv1053728
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)nsv602037
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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