A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528011



Internal ID304085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11021319..11021794hg38UCSC Ensembl
chr20:11001967..11002442hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528011
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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