A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588862



Internal ID21537426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4464674..4468879hg38UCSC Ensembl
chr20:4445321..4449526hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg384206
hg194206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116909
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588862
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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