A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4080n152



Internal ID22819783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3173257..3174061hg38UCSC Ensembl
chr19:3173255..3174059hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3295731, nsv3292175
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv4080n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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