A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8053n152



Internal ID22823756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107953778..107953876hg38UCSC Ensembl
chr6:108274982..108275080hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3285791, nsv3194492
SamplesHG00512, HG00513, HG00514
Known GenesSEC63
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)dgv8053n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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