A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv620263



Internal ID15819618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:61368668..61374668hg38UCSC Ensembl
Outerchr11:61136140..61142140hg19UCSC Ensembl
Outerchr11:60892716..60898716hg18UCSC Ensembl
Outerchr11:60892716..60898716hg17UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv507595
Supporting Variants
SamplesNA15510
Known GenesTMEM138
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)nssv620263
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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