A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524852



Internal ID15105459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:64215039..64329779hg38UCSC Ensembl
Innerchr17:62292399..62407139hg19UCSC Ensembl
Innerchr17:59646131..59760871hg18UCSC Ensembl
Innerchr17:59646131..59760871hg17UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38114741
hg19114741
hg18114741
hg17114741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700854
Samples
Known GenesPECAM1, TEX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524852
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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