A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519992



Internal ID15447285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9916998..9923277hg38UCSC Ensembl
Innerchr11:9938545..9944824hg19UCSC Ensembl
Innerchr11:9895121..9901400hg18UCSC Ensembl
Innerchr11:9895121..9901400hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386280
hg196280
hg186280
hg176280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697166
Samples
Known GenesSBF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519992
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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