A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2136n54



Internal ID20135560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102464878..102545128hg38UCSC Ensembl
chr11:102335609..102415859hg19UCSC Ensembl
chr11:101840819..101921069hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3880251
hg1980251
hg1880251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556151, nsv556150
SamplesHGDP00563, HGDP00570
Known GenesMMP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2136n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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