A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9808n152



Internal ID22825511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134992254..134992319hg38UCSC Ensembl
chr9:137884100..137884165hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3209317, nsv3199178
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9808n152
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