A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018493



Internal ID19107710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9348853..9395912hg38UCSC Ensembl
Innerchr9:9348853..9395912hg19UCSC Ensembl
Innerchr9:9338853..9385912hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3847060
hg1947060
hg1847060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689131, nssv3689130, nssv3689129
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)nsv1018493
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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