A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14455432



Internal ID22215794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102259696..102405716hg38UCSC Ensembl
chrX:101514684..101660637hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38146021
hg19145954
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3549036
Supporting Variants
SamplesHG00733
Known GenesNXF2, NXF2B
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14455432
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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