A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8121n152



Internal ID22823824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137703656..137703793hg38UCSC Ensembl
chr6:138024793..138024930hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3191369, nsv3196812
SamplesNA19238, NA19239, NA19240
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)dgv8121n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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