A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040154



Internal ID21949497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49080128..49080223hg38UCSC Ensembl
chr18:46606498..46606593hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622164
Samples
Known GenesDYM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040154
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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