A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052586



Internal ID21961819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36641900..36642183hg38UCSC Ensembl
chr20:35270303..35270586hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627231
Samples
Known GenesSLA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052586
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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