A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601986



Internal ID16389395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31984179..31988083hg38UCSC Ensembl
Innerchr6:31951956..31955860hg19UCSC Ensembl
Innerchr6:32059935..32063839hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383905
hg193905
hg183905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10469n54
Supporting Variantsnssv1053594
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)nsv601986
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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