A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6055n152



Internal ID22821758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84900405..84915597hg38UCSC Ensembl
chr3:84949556..84964748hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3815193
hg1915193
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3180434, nsv3172057
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv6055n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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