A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6099n152



Internal ID22821802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106073467..106074081hg38UCSC Ensembl
chr3:105792314..105792928hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3282852, nsv3280917
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)dgv6099n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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