A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7421n54



Internal ID22775316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:599013..614136hg38UCSC Ensembl
chr20:579657..594780hg19UCSC Ensembl
chr20:527657..542780hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3815124
hg1915124
hg1815124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv585174, nsv585175
Samples1780862574_A
Known GenesTCF15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7421n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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