A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689133



Internal ID18987414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9385317..9435620hg38UCSC Ensembl
Innerchr9:9385317..9435620hg19UCSC Ensembl
Innerchr9:9375317..9425620hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3850304
hg1950304
hg1850304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015203
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)nssv3689133
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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