A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178100



Internal ID20745140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100760852..100818815hg38UCSC Ensembl
chr14:101227189..101285152hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3857964
hg1957964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508547
Supporting Variants
Samples
Known GenesMIR2392
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178100
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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