A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483000



Internal ID15235474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:10678454..12678453hg38UCSC Ensembl
Outerchr11:10700001..12700000hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382000000
hg192000000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996301
Samples
Known GenesCSNK2A3, CTR9, DKK3, EIF4G2, GALNT18, MICAL2, MICALCL, MIR4299, MIR6124, MIR8070, MRVI1, PARVA, SNORD97, TEAD1, USP47, ZBED5, ZBED5-AS1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483000
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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