A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593224



Internal ID21541810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62992192..62993888hg38UCSC Ensembl
chr20:61623544..61625240hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381697
hg191697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117431
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593224
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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