A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527409



Internal ID15454702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:66731218..66875275hg38UCSC Ensembl
Innerchr10:68490976..68635033hg19UCSC Ensembl
Innerchr10:68160982..68305039hg18UCSC Ensembl
Innerchr10:68160982..68305039hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38144058
hg19144058
hg18144058
hg17144058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703847
Samples
Known GenesCTNNA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527409
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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