A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7840n152



Internal ID22823543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32662530..32662631hg38UCSC Ensembl
chr6:32630307..32630408hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3203713, nsv3198676
SamplesHG00514
Known GenesHLA-DQB1
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)dgv7840n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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