A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519717



Internal ID15100324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33858883..33865001hg38UCSC Ensembl
Innerchr11:33880429..33886547hg19UCSC Ensembl
Innerchr11:33837005..33843123hg18UCSC Ensembl
Innerchr11:33837005..33843123hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg386119
hg196119
hg186119
hg176119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657832, nssv690123
Samples
Known GenesLMO2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519717
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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