A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14457267



Internal ID22211642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76141674..76153292hg38UCSC Ensembl
chrX:75361509..75373127hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3811619
hg1911619
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3556394
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14457267
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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