A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586016



Internal ID16373425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42553671..42614596hg38UCSC Ensembl
Innerchr20:41182311..41243236hg19UCSC Ensembl
Innerchr20:40615725..40676650hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3860926
hg1960926
hg1860926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7577n54
Supporting Variantsnssv939494, nssv939493, nssv939495, nssv939492
Samples
Known GenesPTPRT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586016
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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