A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528169



Internal ID304239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21275657..21281826hg38UCSC Ensembl
chr20:21256295..21262464hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg386170
hg196170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528169
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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