A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180012



Internal ID20747052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58281658..58283371hg38UCSC Ensembl
chr14:58748376..58750089hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381714
hg191714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491276
Supporting Variants
Samples
Known GenesFLJ31306
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180012
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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