A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185846



Internal ID20752886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94682168..94688705hg38UCSC Ensembl
chr14:95148505..95155042hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg386538
hg196538
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504352
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185846
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01135


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