A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186884



Internal ID20753924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98121147..98128951hg38UCSC Ensembl
chr14:98587484..98595288hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg387805
hg197805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186884
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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