A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520437



Internal ID296765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11300871..11302629hg38UCSC Ensembl
chr20:11281519..11283277hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381759
hg191759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520437
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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