A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6369n152



Internal ID22822072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:869568..869633hg38UCSC Ensembl
chr4:863356..863421hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3195605, nsv3202346
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733
Known GenesGAK
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)dgv6369n152
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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