A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8032n152



Internal ID22823735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100931413..100937065hg38UCSC Ensembl
chr6:101379289..101384941hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg385653
hg195653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3207655, nsv3203084
SamplesNA19238, NA19240
Known Genes
MethodOptical mapping
Sequencing
AnalysisBioNano Genomics proprietary analysis
Multiple analysis algorthms
PlatformBioNano Genomics
Illumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8032n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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