A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384907



Internal ID22442777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13857468..13863392hg38UCSC Ensembl
chr18:13857467..13863391hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg385925
hg195925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5946318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384907
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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