A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522491



Internal ID15449784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132814378..132819849hg38UCSC Ensembl
Innerchr10:134627882..134633353hg19UCSC Ensembl
Innerchr10:134477872..134483343hg18UCSC Ensembl
Innerchr10:134477872..134483343hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385472
hg195472
hg185472
hg175472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705858
Samples
Known GenesTTC40
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522491
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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