A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517799



Internal ID15445092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72293947..72296621hg38UCSC Ensembl
Innerchr17:70290088..70292762hg19UCSC Ensembl
Innerchr17:67801683..67804357hg18UCSC Ensembl
Innerchr17:67801683..67804357hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg382675
hg192675
hg182675
hg172675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695202
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517799
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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