A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601255



Internal ID16041978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29931370hg38UCSC Ensembl
Innerchr6:29851443..29899147hg19UCSC Ensembl
Innerchr6:29959422..30007126hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3847705
hg1947705
hg1847705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10344n54
Supporting Variantsnssv1051779
Samples
Known GenesHCG4B, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601255
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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