A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170682



Internal ID22330882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48174010..48175044hg38UCSC Ensembl
chr8:49086570..49087604hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381035
hg191035
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9160n152
Supporting Variantsnssv14460103
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)nsv3170682
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