A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602013



Internal ID16389422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31985690..31993863hg38UCSC Ensembl
Innerchr6:31953467..31961640hg19UCSC Ensembl
Innerchr6:32061446..32069619hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg388174
hg198174
hg188174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10471n54
Supporting Variantsnssv1053657
Samples
Known GenesC4A, C4B, C4B_2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602013
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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