A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2002n54



Internal ID22769897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70230432..70248052hg38UCSC Ensembl
chr11:70076538..70094158hg19UCSC Ensembl
chr11:69754186..69771806hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3817621
hg1917621
hg1817621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555384, nsv555393, nsv555395, nsv555383
SamplesHGDP00262, HGDP00017
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2002n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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