A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590821



Internal ID21539391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46819768..46829535hg38UCSC Ensembl
chr20:45448407..45458174hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg389768
hg199768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116703
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590821
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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