A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186805



Internal ID20753845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99746316..100046234hg38UCSC Ensembl
chr14:100212653..100512571hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38299919
hg19299919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496453
Supporting Variants
Samples
Known GenesEML1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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