A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv357n152



Internal ID22816060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105571333..105573592hg38UCSC Ensembl
chr1:106113955..106116214hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg382260
hg192260
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3184722, nsv3172608, nsv3186337
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)dgv357n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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