A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191786



Internal ID22342446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139013406..139013697hg38UCSC Ensembl
chr3:138732248..138732539hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14309487
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191786
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