A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519434



Internal ID15446727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122083008..122086975hg38UCSC Ensembl
Innerchr10:123842523..123846490hg19UCSC Ensembl
Innerchr10:123832513..123836480hg18UCSC Ensembl
Innerchr10:123832513..123836480hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383968
hg193968
hg183968
hg173968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656193, nssv689058
Samples
Known GenesTACC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519434
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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