A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629947



Internal ID21821994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45777094..45779308hg38UCSC Ensembl
chr18:43357059..43359273hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg382215
hg192215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629947
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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