A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2203n54



Internal ID20135627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132949989..133394114hg38UCSC Ensembl
chr11:132819884..133264009hg19UCSC Ensembl
chr11:132325094..132769219hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38444126
hg19444126
hg18444126
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556591, nsv556590
Samples
Known GenesOPCML
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2203n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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