A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7576n54



Internal ID22775471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42529067..42669053hg38UCSC Ensembl
chr20:41157707..41297693hg19UCSC Ensembl
chr20:40591121..40731107hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38139987
hg19139987
hg18139987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586006, nsv586018
Samples
Known GenesPTPRT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7576n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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