A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6360n152



Internal ID22822063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:651687..651759hg38UCSC Ensembl
chr4:645476..645548hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3201163, nsv3206274
SamplesNA19239, NA19240
Known GenesPDE6B
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)dgv6360n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer