A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516502



Internal ID15443795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124996775..125004911hg38UCSC Ensembl
Innerchr10:126685344..126693480hg19UCSC Ensembl
Innerchr10:126675334..126683470hg18UCSC Ensembl
Innerchr10:126675334..126683470hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg388137
hg198137
hg188137
hg178137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv51n21
Supporting Variantsnssv686802, nssv668716
Samples
Known GenesCTBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516502
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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