A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439683



Internal ID22236346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6321385..6321444hg38UCSC Ensembl
chrX:6239426..6239485hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3188108
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)nssv14439683
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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