A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519716



Internal ID15447009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9020223..9022205hg38UCSC Ensembl
Innerchr9:9020223..9022205hg19UCSC Ensembl
Innerchr9:9010223..9012205hg18UCSC Ensembl
Innerchr9:9010223..9012205hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381983
hg191983
hg181983
hg171983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697009
Samples
Known GenesPTPRD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519716
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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