A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222566



Internal ID22366602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104905183..104905398hg38UCSC Ensembl
chr14:105371520..105371735hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2778n152
Supporting Variantsnssv14458185
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)nsv3222566
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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