A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3543794



Internal ID22412843
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14462332, nssv14463547
SamplesNA19238, NA19240
Known GenesRHOXF1, RHOXF2, RHOXF2B
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3543794
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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