A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14406660



Internal ID22312752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25762814..25846589hg38UCSC Ensembl
chr20:25743450..25827225hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3883776
hg1983776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225958
Supporting Variants
SamplesNA19240
Known GenesFAM182B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14406660
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