A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586009



Internal ID16373418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42545465..42626053hg38UCSC Ensembl
Innerchr20:41174105..41254693hg19UCSC Ensembl
Innerchr20:40607519..40688107hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3880589
hg1980589
hg1880589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7577n54
Supporting Variantsnssv939485
Samples
Known GenesPTPRT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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