A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509874



Internal ID20883187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99642549..99643064hg38UCSC Ensembl
chr14:100108886..100109401hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38516
hg19516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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