A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6908n54



Internal ID20140332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60756834..60892336hg38UCSC Ensembl
chr2:60983969..61119471hg19UCSC Ensembl
chr2:60837473..60972975hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38135503
hg19135503
hg18135503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582117, nsv582116
Samples
Known GenesFLJ16341, PAPOLG, REL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6908n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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