A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516433



Internal ID15097040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9017282..9023857hg38UCSC Ensembl
Innerchr17:8920599..8927174hg19UCSC Ensembl
Innerchr17:8861324..8867899hg18UCSC Ensembl
Innerchr17:8861324..8867899hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386576
hg196576
hg186576
hg176576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668334, nssv693309
Samples
Known GenesNTN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516433
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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