A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060878



Internal ID18803409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:42688542..42713650hg38UCSC Ensembl
Innerchr20:41317182..41342290hg19UCSC Ensembl
Innerchr20:40750596..40775704hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3825109
hg1925109
hg1825109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584827
Samples
Known GenesPTPRT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060878
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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