A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7326n54



Internal ID22775221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:228501467..228566625hg38UCSC Ensembl
chr2:229366183..229431341hg19UCSC Ensembl
chr2:229074427..229139585hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3865159
hg1965159
hg1865159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv584629, nsv584630
SamplesHGDP00470, HGDP00451, HGDP00458, HGDP00464
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7326n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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