A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126931



Internal ID15633431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9801907..9859571hg38UCSC Ensembl
Innerchr9:9801907..9859571hg19UCSC Ensembl
Innerchr9:9791907..9849571hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3857665
hg1957665
hg1857665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613338
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)nssv1126931
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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