A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6950n54



Internal ID22774845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89026617..90239257hg38UCSC Ensembl
chr2:89326114..90278124hg19UCSC Ensembl
chr2:89107229..89915429hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381212641
hg19952011
hg18808201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582396, nsv582399, nsv582398
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6950n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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