A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14465073



Internal ID22144129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154346996..154385012hg38UCSC Ensembl
chrX:153575364..153613372hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3838017
hg1938009
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3554245
Supporting Variants
SamplesHG00514
Known GenesEMD, FLNA
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14465073
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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