A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598265



Internal ID21546889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56188986..56189162hg38UCSC Ensembl
chr20:54764042..54764218hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117001
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598265
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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