A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8065n152



Internal ID22823768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113621725..113621827hg38UCSC Ensembl
chr6:113942927..113943029hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3283769, nsv3193220
SamplesNA19238, HG00731, NA19240, HG00513, 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)dgv8065n152
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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