A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14456021



Internal ID22284837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63182029..63198950hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3816922
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3554042
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14456021
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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