A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517312



Internal ID293738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3317876..3331928hg38UCSC Ensembl
chr20:3298523..3312575hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3814053
hg1914053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17730408
Samples
Known GenesC20orf194
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517312
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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