A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521810



Internal ID15449103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87323654..87326638hg38UCSC Ensembl
Innerchr11:87034696..87037680hg19UCSC Ensembl
Innerchr11:86712344..86715328hg18UCSC Ensembl
Innerchr11:86712344..86715328hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382985
hg192985
hg182985
hg172985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694580
Samples
Known GenesTMEM135
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521810
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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