A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407986



Internal ID22465856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9686857..9689023hg38UCSC Ensembl
chr18:9686854..9689020hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg382167
hg192167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5942392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407986
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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