A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523644



Internal ID15450937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124995565..125004911hg38UCSC Ensembl
Innerchr10:126684134..126693480hg19UCSC Ensembl
Innerchr10:126674124..126683470hg18UCSC Ensembl
Innerchr10:126674124..126683470hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg389347
hg199347
hg189347
hg179347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv51n21
Supporting Variantsnssv699445
Samples
Known GenesCTBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523644
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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