A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5895n152



Internal ID22821598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20301220..20301402hg38UCSC Ensembl
chr3:20342712..20342894hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3181649, nsv3178200
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)dgv5895n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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