A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14465776



Internal ID22260008
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3552538
Supporting Variants
SamplesNA19238
Known GenesHSFX1, HSFX2
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14465776
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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