A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175428



Internal ID22333357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79864708..79864785hg38UCSC Ensembl
chrX:79120208..79120285hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14385946
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)nsv3175428
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer