A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519762



Internal ID296108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34777872..34781258hg38UCSC Ensembl
chr20:33365675..33369061hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383387
hg193387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732125
Samples
Known GenesNCOA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519762
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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