A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209718



Internal ID22357748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24209057..24209139hg38UCSC Ensembl
chr14:24678263..24678345hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14444955
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)nsv3209718
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