A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526471



Internal ID15107078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9718066..9832245hg38UCSC Ensembl
Innerchr9:9718066..9832245hg19UCSC Ensembl
Innerchr9:9708066..9822245hg18UCSC Ensembl
Innerchr9:9708066..9822245hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38114180
hg19114180
hg18114180
hg17114180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702775
Samples
Known GenesPTPRD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526471
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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