A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv509442



Internal ID15825468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:110504432..110515648hg38UCSC Ensembl
Outerchr11:110375156..110386372hg19UCSC Ensembl
Outerchr11:109880366..109891582hg18UCSC Ensembl
Outerchr11:109880366..109891582hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383318
hg193318
hg183318
hg173318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv619458
SamplesNA10860
Known Genes
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)nsv509442
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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