A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7422n54



Internal ID20140846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:606311..613017hg38UCSC Ensembl
chr20:586955..593661hg19UCSC Ensembl
chr20:534955..541661hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386707
hg196707
hg186707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585178, nsv585177
Samples
Known GenesTCF15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7422n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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