A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189867



Internal ID20756907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104495243..104586301hg38UCSC Ensembl
chr14:104961580..105052638hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3891059
hg1991059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495602
Supporting Variants
Samples
Known GenesC14orf180
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189867
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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