A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3554042



Internal ID22422911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63182029..63198950hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3816922
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14460365, nssv14456021, nssv14456739, nssv14463686
SamplesNA19238, NA19239, NA19240, HG00513
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3554042
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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