A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351180



Internal ID22231237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49157254..49162986hg38UCSC Ensembl
chrX:49013593..49019324hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg385733
hg195732
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230668
Supporting Variants
SamplesHG00733
Known GenesMAGIX
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351180
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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