A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4392n152



Internal ID22820095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58410519..58410764hg38UCSC Ensembl
chr19:58921886..58922131hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3296951, nsv3298232, nsv3296894
SamplesNA19240, HG00733, HG00514
Known GenesZNF584
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv4392n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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