A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523896



Internal ID300112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62632193..62634445hg38UCSC Ensembl
chr20:61263545..61265797hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382253
hg192253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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