A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427882



Internal ID206774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5170228..5170279hg38UCSC Ensembl
chr20:5150874..5150925hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730546
Samples
Known GenesCDS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427882
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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