A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054980



Internal ID21964213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21305474..21308134hg38UCSC Ensembl
chr20:21286112..21288772hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382661
hg192661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635183
Samples
Known GenesXRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054980
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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