A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3552538



Internal ID22421433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149742318..149776625hg38UCSC Ensembl
chrX:148823979..148858283hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3834308
hg1934305
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14467500, nssv14453103, nssv14465776
SamplesHG00512, NA19238, HG00514
Known GenesHSFX1, HSFX2
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3552538
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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