A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv976n152



Internal ID22816679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69409866..69409918hg38UCSC Ensembl
chr10:71169622..71169674hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3285007, nsv3222424
SamplesNA19238, HG00731, HG00732, HG00733
Known GenesTACR2
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv976n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer