A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499036



Internal ID20872252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88989467..89005949hg38UCSC Ensembl
chr14:89455811..89472293hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3816483
hg1916483
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190158
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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