A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126881



Internal ID15980067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8408453..8422302hg38UCSC Ensembl
Innerchr9:8408453..8422302hg19UCSC Ensembl
Innerchr9:8398453..8412302hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3813850
hg1913850
hg1813850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613287
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126881
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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