A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126919



Internal ID15633419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9796116..9803954hg38UCSC Ensembl
Innerchr9:9796116..9803954hg19UCSC Ensembl
Innerchr9:9786116..9793954hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg387839
hg197839
hg187839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613328
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)nssv1126919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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