A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939491



Internal ID16233447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42553671..42612060hg38UCSC Ensembl
Innerchr20:41182311..41240700hg19UCSC Ensembl
Innerchr20:40615725..40674114hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3858390
hg1958390
hg1858390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586015
Supporting Variants
Samples
Known GenesPTPRT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939491
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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