A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601298



Internal ID16042021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29888682..29942940hg38UCSC Ensembl
Innerchr6:29856459..29910717hg19UCSC Ensembl
Innerchr6:29964438..30018696hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3854259
hg1954259
hg1854259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10347n54
Supporting Variantsnssv1051848
Samples
Known GenesHCG4B, HLA-A, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601298
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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