A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629964



Internal ID21822011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21156374..21160184hg38UCSC Ensembl
chr18:18736335..18740145hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg383811
hg193811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039140
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629964
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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