A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8132n152



Internal ID22823835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141433621..141433697hg38UCSC Ensembl
chr6:141754758..141754834hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3284779, nsv3528497
SamplesHG00732, HG00733
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)dgv8132n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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