A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519650



Internal ID15100257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18234974..18235470hg38UCSC Ensembl
Innerchr11:18256521..18257017hg19UCSC Ensembl
Innerchr11:18213097..18213593hg18UCSC Ensembl
Innerchr11:18213097..18213593hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38497
hg19497
hg18497
hg17497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694074
Samples
Known GenesSAA2-SAA4, SAA4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519650
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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