A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126923



Internal ID15633423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9798092..9869714hg38UCSC Ensembl
Innerchr9:9798092..9869714hg19UCSC Ensembl
Innerchr9:9788092..9859714hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3871623
hg1971623
hg1871623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613332
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)nssv1126923
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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