A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533242



Internal ID309138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3859940..3861036hg38UCSC Ensembl
chr20:3840587..3841683hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381097
hg191097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730459
Samples
Known GenesMAVS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533242
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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