A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529779



Internal ID305785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56785247..56790029hg38UCSC Ensembl
chr20:55360303..55365085hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg384783
hg194783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529779
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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