A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7262n54



Internal ID22775157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203318233..203327478hg38UCSC Ensembl
chr2:204182956..204192201hg19UCSC Ensembl
chr2:203891201..203900446hg18UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg389246
hg199246
hg189246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv584230, nsv584236, nsv584234, nsv584231, nsv584238, nsv584233, nsv584239, nsv584235, nsv584237
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7262n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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