A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206817



Internal ID22355306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68866111..68868257hg38UCSC Ensembl
chr14:69332828..69334974hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382147
hg192147
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2657n152
Supporting Variantsnssv14417516, nssv14390347
SamplesNA19240, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206817
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