A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510882



Internal ID15478376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:48526907..48577669hg38UCSC Ensembl
Outerchr19:49030164..49080926hg19UCSC Ensembl
Outerchr19:53721976..53772738hg18UCSC Ensembl
Outerchr19:53721976..53772738hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3850763
hg1950763
hg1850763
hg1750763
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv621647
SamplesNA15510
Known GenesSULT2B1
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)nsv510882
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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