A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630431



Internal ID21822478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:30868636..30868879hg38UCSC Ensembl
chr18:28448602..28448845hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033276
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630431
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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