A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6930n54



Internal ID22774825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77760423..77814957hg38UCSC Ensembl
chr2:77987549..78042083hg19UCSC Ensembl
chr2:77841057..77895591hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3854535
hg1954535
hg1854535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv582265, nsv582264, nsv582266
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6930n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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