A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602072



Internal ID16042795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32011830..32037490hg38UCSC Ensembl
Innerchr6:31979607..32005267hg19UCSC Ensembl
Innerchr6:32087585..32113246hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3825661
hg1925661
hg1825662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053817
Samples
Known GenesC4A, C4B, C4B_2, STK19, TNXA, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602072
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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