A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8144n152



Internal ID22823847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150320841..150326955hg38UCSC Ensembl
chr6:150641977..150648091hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg386115
hg196115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3206578, nsv3198839
SamplesNA19239, 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)dgv8144n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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