A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2202n54



Internal ID20135626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132057409..132060294hg38UCSC Ensembl
chr11:131927303..131930188hg19UCSC Ensembl
chr11:131432513..131435398hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382886
hg192886
hg182886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556584, nsv556585, nsv556586
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2202n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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