A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528579



Internal ID304631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53628764..53630385hg38UCSC Ensembl
chr20:52245303..52246924hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381622
hg191622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528579
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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