A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528666



Internal ID15455959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72660591..72662130hg38UCSC Ensembl
Innerchr17:70656730..70658269hg19UCSC Ensembl
Innerchr17:68168325..68169864hg18UCSC Ensembl
Innerchr17:68168325..68169864hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381540
hg191540
hg181540
hg171540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705304
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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