A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459019



Internal ID22252788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149102242..149102527hg38UCSC Ensembl
chrX:148183772..148184057hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3189419
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459019
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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