A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054356



Internal ID21963589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19678458..19678510hg38UCSC Ensembl
chr20:19659102..19659154hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626948
Samples
Known GenesSLC24A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054356
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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