A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518851



Internal ID15099458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9798666..9819028hg38UCSC Ensembl
Innerchr9:9798666..9819028hg19UCSC Ensembl
Innerchr9:9788666..9809028hg18UCSC Ensembl
Innerchr9:9788666..9809028hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3820363
hg1920363
hg1820363
hg1720363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696304
Samples
Known GenesPTPRD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518851
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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