A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516040



Internal ID15096647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78458739..78459795hg38UCSC Ensembl
Innerchr11:78169785..78170841hg19UCSC Ensembl
Innerchr11:77847433..77848489hg18UCSC Ensembl
Innerchr11:77847433..77848489hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381057
hg191057
hg181057
hg171057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673780, nssv653947
Samples
Known GenesNARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516040
Frequency
Sample Size2026
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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