A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516382



Internal ID15443675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20047418..20056950hg38UCSC Ensembl
Innerchr11:20068964..20078496hg19UCSC Ensembl
Innerchr11:20025540..20035072hg18UCSC Ensembl
Innerchr11:20025540..20035072hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg389533
hg199533
hg189533
hg179533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv668503, nssv667933
Samples
Known GenesNAV2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516382
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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