A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180927



Internal ID22336313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115694145..115720850hg38UCSC Ensembl
chrX:114928465..114955170hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3826706
hg1926706
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14429210
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3180927
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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