A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526271



Internal ID15453564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70110847..70119912hg38UCSC Ensembl
Innerchr17:68106988..68116053hg19UCSC Ensembl
Innerchr17:65618583..65627648hg18UCSC Ensembl
Innerchr17:65618583..65627648hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg389066
hg199066
hg189066
hg179066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702545
Samples
Known GenesKCNJ16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526271
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer