A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516087



Internal ID15443380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66748578..66812101hg38UCSC Ensembl
Innerchr11:66516049..66579572hg19UCSC Ensembl
Innerchr11:66272625..66336148hg18UCSC Ensembl
Innerchr11:66272625..66336148hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3863524
hg1963524
hg1863524
hg1763524
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688545, nssv663664, nssv680957, nssv676680, nssv666120, nssv682696, nssv667561
Samples
Known GenesC11orf80
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516087
Frequency
Sample Size2026
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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