A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3243898



Internal ID22375706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12141461..12150226hg38UCSC Ensembl
chr18:12141460..12150225hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg388766
hg198766
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14467583, nssv14454718, nssv14457730, nssv14459577, nssv14462239, nssv14465000, nssv14453364, nssv14457545
SamplesHG00512, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3243898
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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