A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6867n54



Internal ID22774762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:51080937..51288534hg38UCSC Ensembl
chr2:51308075..51515672hg19UCSC Ensembl
chr2:51161579..51369176hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38207598
hg19207598
hg18207598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581873, nsv581870
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6867n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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