A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636721



Internal ID21828768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48947008..48947284hg38UCSC Ensembl
chr18:46473378..46473654hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027517
Supporting Variants
Samples
Known GenesSMAD7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636721
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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