A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14407400



Internal ID22300749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41140521..41140782hg38UCSC Ensembl
chr19:41646426..41646687hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210632
Supporting Variants
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)nssv14407400
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