A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042575



Internal ID21951891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16582225..16691148hg38UCSC Ensembl
chr20:16562870..16671793hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38108924
hg19108924
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042575
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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