A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373677



Internal ID22599346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25466956..25488272hg38UCSC Ensembl
chr18:23046920..23068236hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3821317
hg1921317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5933506
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373677
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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