A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518777



Internal ID15099384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6895059..6898945hg38UCSC Ensembl
Innerchr17:6798378..6802264hg19UCSC Ensembl
Innerchr17:6739102..6742988hg18UCSC Ensembl
Innerchr17:6739102..6742988hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383887
hg193887
hg183887
hg173887
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696230
Samples
Known GenesALOX12P2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518777
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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