A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511064



Internal ID15827086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:25852971..26003449hg38UCSC Ensembl
Outerchr20:25833607..25984085hg19UCSC Ensembl
Outerchr20:25781607..25932085hg18UCSC Ensembl
Outerchr20:25781607..25932085hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38150479
hg19150479
hg18150479
hg17150479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv622430
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)nsv511064
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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