A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188296



Internal ID22340173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152707443..152744003hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3836561
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387578, nssv14376443
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)nsv3188296
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