A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524497



Internal ID300704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24822065..24822784hg38UCSC Ensembl
chr20:24802701..24803420hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524497
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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