A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522986



Internal ID299237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50755806..50755884hg38UCSC Ensembl
chr20:49372343..49372421hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522986
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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