A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14403167



Internal ID22293943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40823261..40823458hg38UCSC Ensembl
chrX:40682514..40682711hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3176925
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)nssv14403167
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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