A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6305n152



Internal ID22822008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189501128..189501196hg38UCSC Ensembl
chr3:189218917..189218985hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3210232, nsv3204601
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)dgv6305n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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