A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590810



Internal ID21539380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21022067..21022414hg38UCSC Ensembl
chr20:21002708..21003055hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116251
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590810
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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