A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6668n54



Internal ID22774563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4165788..4197930hg38UCSC Ensembl
chr2:4213378..4245520hg19UCSC Ensembl
chr2:4191253..4223395hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3832143
hg1932143
hg1832143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580843, nsv580844
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6668n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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