A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520832



Internal ID15448125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9326805..9364637hg38UCSC Ensembl
Innerchr9:9326805..9364637hg19UCSC Ensembl
Innerchr9:9316805..9354637hg18UCSC Ensembl
Innerchr9:9316805..9354637hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3837833
hg1937833
hg1837833
hg1737833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697640
Samples
Known GenesPTPRD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520832
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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