A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14462332



Internal ID22262133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120075637..120172547hg38UCSC Ensembl
chrX:119209602..119306402hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3896911
hg1996801
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3543794
Supporting Variants
SamplesNA19238
Known GenesRHOXF1, RHOXF2, RHOXF2B
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14462332
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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