A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3548744



Internal ID22417694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135713409..135798324hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3884916
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14461350, nssv14464472
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3548744
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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