A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385274



Internal ID22443144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97700499..97709555hg38UCSC Ensembl
chr14:98166836..98175892hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg389057
hg199057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385274
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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