A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2061n54



Internal ID22769956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89011248..89125229hg38UCSC Ensembl
chr11:88744416..88858397hg19UCSC Ensembl
chr11:88384064..88498045hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38113982
hg19113982
hg18113982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555734, nsv555732, nsv555733
SamplesHGDP00639, HGDP01343
Known GenesGRM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2061n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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