A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6898n54



Internal ID22774793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:56485291..56527344hg38UCSC Ensembl
chr2:56712426..56754479hg19UCSC Ensembl
chr2:56565930..56607983hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3842054
hg1942054
hg1842054
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582054, nsv582052, nsv582053
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6898n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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