A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517566



Internal ID293986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34035121..34035231hg38UCSC Ensembl
chr20:32622927..32623037hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732061
Samples
Known GenesRALY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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