A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236455



Internal ID22373581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10806629..10809752hg38UCSC Ensembl
chr20:10787277..10790400hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg383124
hg193124
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14464417, nssv14463742, nssv14460567
SamplesHG00512, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236455
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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