A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170918



Internal ID22331003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40712256..40712938hg38UCSC Ensembl
chr3:40753747..40754429hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459625
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)nsv3170918
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