A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056713



Internal ID21965947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19678275..19678408hg38UCSC Ensembl
chr20:19658919..19659052hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628710
Samples
Known GenesSLC24A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056713
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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