A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517639



Internal ID15444932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9119229..9119349hg38UCSC Ensembl
Innerchr9:9119229..9119349hg19UCSC Ensembl
Innerchr9:9109229..9109349hg18UCSC Ensembl
Innerchr9:9109229..9109349hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38121
hg19121
hg18121
hg17121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671734, nssv689782
Samples
Known GenesPTPRD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517639
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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