A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453580



Internal ID22217698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52489201..52533696hg38UCSC Ensembl
chrX:52232344..52562706hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3844496
hg19330363
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3231746
Supporting Variants
SamplesHG00733
Known GenesXAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14453580
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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