A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689132



Internal ID18987413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9385317..9395912hg38UCSC Ensembl
Innerchr9:9385317..9395912hg19UCSC Ensembl
Innerchr9:9375317..9385912hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3810596
hg1910596
hg1810596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029346
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3689132
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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