A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3555201



Internal ID22424044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66250101..66253619hg38UCSC Ensembl
chr11:66017572..66021090hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383519
hg193519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14462843
SamplesHG00732
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3555201
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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