A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3247663



Internal ID22376599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153121931..153292732hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38170802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14452589, nssv14459575, nssv14463727, nssv14456252, nssv14464350, nssv14455863
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3247663
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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