A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6010n152



Internal ID22821713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72447089..72447581hg38UCSC Ensembl
chr3:72496240..72496732hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3178708, nsv3189628, nsv3180377
SamplesNA19240, HG00733, 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)dgv6010n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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