A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528425



Internal ID15455718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9437674..9556992hg38UCSC Ensembl
Innerchr9:9437674..9556992hg19UCSC Ensembl
Innerchr9:9427674..9546992hg18UCSC Ensembl
Innerchr9:9427674..9546992hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38119319
hg19119319
hg18119319
hg17119319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705018
Samples
Known GenesPTPRD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528425
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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