A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7577n54



Internal ID22775472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42545465..42632804hg38UCSC Ensembl
chr20:41174105..41261444hg19UCSC Ensembl
chr20:40607519..40694858hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3887340
hg1987340
hg1887340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586013, nsv586016, nsv586014, nsv586015, nsv586009, nsv586012, nsv586011, nsv586017
Samples
Known GenesPTPRT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7577n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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