A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8057n152



Internal ID22823760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110600712..110605302hg38UCSC Ensembl
chr6:110921915..110926505hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384591
hg194591
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3248194, nsv3230416
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)dgv8057n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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