A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636801



Internal ID21828848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62384316..62384389hg38UCSC Ensembl
chr18:60051549..60051622hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028277
Supporting Variants
Samples
Known GenesTNFRSF11A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636801
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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