A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518907



Internal ID15446200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124993119..125002611hg38UCSC Ensembl
Innerchr10:126681688..126691180hg19UCSC Ensembl
Innerchr10:126671678..126681170hg18UCSC Ensembl
Innerchr10:126671678..126681170hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg389493
hg199493
hg189493
hg179493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696365
Samples
Known GenesCTBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518907
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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