A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613333



Internal ID16054056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9798666..9819028hg38UCSC Ensembl
Innerchr9:9798666..9819028hg19UCSC Ensembl
Innerchr9:9788666..9809028hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3820363
hg1920363
hg1820363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12508n54
Supporting Variantsnssv1126925, nssv1126926, nssv1126924
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613333
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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