A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514988



Internal ID291477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62608625..62608681hg38UCSC Ensembl
chr20:61205832..61205888hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514988
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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