A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510278



Internal ID15477776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:122923914..122929914hg38UCSC Ensembl
Outerchr11:122794622..122800622hg19UCSC Ensembl
Outerchr11:122299832..122305832hg18UCSC Ensembl
Outerchr11:122299832..122305832hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv618355
SamplesCHM
Known GenesC11orf63
MethodOptical mapping
AnalysisSingle-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence.
PlatformOptical Mapping
Comments
ReferenceTeague_et_al_2010
Pubmed ID20534489
Accession Number(s)nsv510278
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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