A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2803n54



Internal ID22770698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95617664..95618311hg38UCSC Ensembl
chr12:96011440..96012087hg19UCSC Ensembl
chr12:94535571..94536218hg18UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38648
hg19648
hg18648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv559829, nsv559828
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2803n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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