A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388834



Internal ID22446704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34929445..34929733hg38UCSC Ensembl
chr18:32509409..32509697hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932851
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388834
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004


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