A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4239n152



Internal ID22819942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32664906..32665310hg38UCSC Ensembl
chr19:33155812..33156216hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3228796, nsv3222409
SamplesNA19240
Known GenesANKRD27
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)dgv4239n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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