A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6048147



Internal ID21957380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35220222..35221263hg38UCSC Ensembl
chr20:33808025..33809066hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6048147
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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