A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10439n54



Internal ID22778334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31340853..31359557hg38UCSC Ensembl
chr6:31308630..31327334hg19UCSC Ensembl
chr6:31416609..31435313hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3818705
hg1918705
hg1818705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv601822, nsv601821
SamplesHGDP00491
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10439n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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