A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3185492



Internal ID22338703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53293790..53294252hg38UCSC Ensembl
chr3:53327820..53328282hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14396282
SamplesNA19240
Known GenesDCP1A
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3185492
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