A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033818



Internal ID21943161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9397901..9397960hg38UCSC Ensembl
chr18:9397899..9397958hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617928
Samples
Known GenesTWSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033818
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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