A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523703



Internal ID299928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33861852..33881239hg38UCSC Ensembl
chr20:32449658..32469045hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3819388
hg1919388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523703
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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