A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14403161



Internal ID22292066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39116804..39116936hg38UCSC Ensembl
chrX:38976057..38976189hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3171993
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)nssv14403161
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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