A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515868



Internal ID15096475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82874314..82981480hg38UCSC Ensembl
Innerchr11:82585356..82692522hg19UCSC Ensembl
Innerchr11:82263004..82370170hg18UCSC Ensembl
Innerchr11:82263004..82370170hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38107167
hg19107167
hg18107167
hg17107167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665090, nssv663774
Samples
Known GenesC11orf82, PRCP, RAB30
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515868
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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