A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196896



Internal ID22346836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26926021..26926230hg38UCSC Ensembl
chr12:27078954..27079163hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390948
SamplesNA19240
Known GenesASUN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196896
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