A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525293



Internal ID15105900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8847233..8850071hg38UCSC Ensembl
Innerchr9:8847233..8850071hg19UCSC Ensembl
Innerchr9:8837233..8840071hg18UCSC Ensembl
Innerchr9:8837233..8840071hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382839
hg192839
hg182839
hg172839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701399
Samples
Known GenesPTPRD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525293
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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