A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636522



Internal ID21828569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23331986..23332127hg38UCSC Ensembl
chr18:20911950..20912091hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038007
Supporting Variants
Samples
Known GenesTMEM241
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636522
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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