A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520150



Internal ID15100757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124871876..124889152hg38UCSC Ensembl
Innerchr11:124741772..124759048hg19UCSC Ensembl
Innerchr11:124246982..124264258hg18UCSC Ensembl
Innerchr11:124246982..124264258hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3817277
hg1917277
hg1817277
hg1717277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697250
Samples
Known GenesROBO3, ROBO4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520150
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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