A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14353105



Internal ID22233281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:98301513..98429194hg38UCSC Ensembl
chrX:97556511..97684192hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38127682
hg19127682
Variant TypeOTHER complex substitution
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3520992
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14353105
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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