A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14462576



Internal ID22191829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101597522..101616276hg38UCSC Ensembl
chrX:100852500..100871266hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3818755
hg1918767
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3246826
Supporting Variants
SamplesHG00731
Known GenesARMCX6
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14462576
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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