A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028474



Internal ID21937817
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 StatusM
Merged Variants
Supporting Variantsnssv17629327
Samples
Known GenesTWSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028474
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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