A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2970n152



Internal ID22818673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68691312..68691625hg38UCSC Ensembl
chr15:68983651..68983964hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3177437, nsv3181679
SamplesNA19240, HG00733, HG00514
Known GenesCORO2B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2970n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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