A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015898



Internal ID18758432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8753534..9011443hg38UCSC Ensembl
Innerchr9:8753534..9011443hg19UCSC Ensembl
Innerchr9:8743534..9001443hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38257910
hg19257910
hg18257910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758121
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)nsv1015898
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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