A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025345



Internal ID21934688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56523658..56535555hg38UCSC Ensembl
chr18:54190889..54202786hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3811898
hg1911898
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025345
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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