A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2000n54



Internal ID22769895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70225821..70253896hg38UCSC Ensembl
chr11:70071927..70100002hg19UCSC Ensembl
chr11:69749575..69777650hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3828076
hg1928076
hg1828076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555378, nsv555385
SamplesHGDP00520
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2000n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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