A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526398



Internal ID15453691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:69403701..69404227hg38UCSC Ensembl
Innerchr14:69870418..69870944hg19UCSC Ensembl
Innerchr14:68940171..68940697hg18UCSC Ensembl
Innerchr14:68940171..68940697hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38527
hg19527
hg18527
hg17527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702697
Samples
Known GenesSLC39A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526398
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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