A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10393n54



Internal ID20143817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31308974..31483699hg38UCSC Ensembl
chr6:31276751..31451476hg19UCSC Ensembl
chr6:31384730..31559455hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38174726
hg19174726
hg18174726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601570, nsv601660
Samples
Known GenesHCG26, HCP5, HLA-B, MICA, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10393n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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