A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14404268



Internal ID22290288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22019089..22024122hg38UCSC Ensembl
chrX:22037207..22042240hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg385034
hg195034
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3173036
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14404268
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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