A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14458773



Internal ID22252584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55464229..55511347hg38UCSC Ensembl
chrX:55490662..55537780hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3847119
hg1947119
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3247799
Supporting Variants
SamplesHG00733
Known GenesUSP51
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14458773
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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