A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520759



Internal ID15448052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133030314..133038096hg38UCSC Ensembl
Innerchr9:135905701..135913483hg19UCSC Ensembl
Innerchr9:134895522..134903304hg18UCSC Ensembl
Innerchr9:132935255..132943037hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg387783
hg197783
hg187783
hg177783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697594
Samples
Known GenesGTF3C5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520759
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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