A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519640



Internal ID15100247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76162361..76183065hg38UCSC Ensembl
Innerchr10:77922119..77942823hg19UCSC Ensembl
Innerchr10:77592125..77612829hg18UCSC Ensembl
Innerchr10:77592125..77612829hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3820705
hg1920705
hg1820705
hg1720705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696966
Samples
Known GenesC10orf11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519640
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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