A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8201n152



Internal ID22823904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163593841..163594196hg38UCSC Ensembl
chr6:164014873..164015228hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3187149, nsv3183250
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv8201n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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