A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8210n152



Internal ID22823913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166221906..166221978hg38UCSC Ensembl
chr6:166635394..166635466hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3284004, nsv3207625, nsv3285498
SamplesNA19240, 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)dgv8210n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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