A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6086n152



Internal ID22821789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99263576..99263652hg38UCSC Ensembl
chr3:98982420..98982496hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3525362, nsv3282372
SamplesHG00512, HG00732, HG00733, HG00513, HG00514
Known Genes
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)dgv6086n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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