A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518583



Internal ID15445876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19971251..19997212hg38UCSC Ensembl
Innerchr11:19992797..20018758hg19UCSC Ensembl
Innerchr11:19949373..19975334hg18UCSC Ensembl
Innerchr11:19949373..19975334hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3825962
hg1925962
hg1825962
hg1725962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696028
Samples
Known GenesNAV2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518583
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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