A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586076



Internal ID21534626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8406021..8409849hg38UCSC Ensembl
chr19:8470905..8474733hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383829
hg193829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106732
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586076
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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