A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8301n152



Internal ID22824004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170632773..170684783hg38UCSC Ensembl
chr6:170941861..170993871hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3852011
hg1952011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3192024, nsv3209266
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8301n152
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer