A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520770



Internal ID15448063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125006700..125007104hg38UCSC Ensembl
Innerchr10:126695269..126695673hg19UCSC Ensembl
Innerchr10:126685259..126685663hg18UCSC Ensembl
Innerchr10:126685259..126685663hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38405
hg19405
hg18405
hg17405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694400
Samples
Known GenesCTBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520770
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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