A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586017



Internal ID16373426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42553671..42632804hg38UCSC Ensembl
Innerchr20:41182311..41261444hg19UCSC Ensembl
Innerchr20:40615725..40694858hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3879134
hg1979134
hg1879134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7577n54
Supporting Variantsnssv939496
Samples
Known GenesPTPRT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586017
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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