A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11953n54



Internal ID22779848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10678316..10710120hg38UCSC Ensembl
chr8:10535826..10567630hg19UCSC Ensembl
chr8:10573236..10605040hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3831805
hg1931805
hg1831805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610273, nsv610272
Samples1780854535_A, HGDP00515
Known GenesC8orf74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11953n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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