A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629327



Internal ID21821374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9351627..9351696hg38UCSC Ensembl
chr18:9351625..9351694hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028474
Supporting Variants
Samples
Known GenesTWSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629327
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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