A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6345n152



Internal ID22822048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197030146..197030399hg38UCSC Ensembl
chr3:196757017..196757270hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3195986, nsv3280551
SamplesHG00513, 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)dgv6345n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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