A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629009



Internal ID21821056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:626928..627007hg38UCSC Ensembl
chr18:626928..627007hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036433
Supporting Variants
Samples
Known GenesCLUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629009
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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