A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480382



Internal ID21137935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85332787..85383663hg38UCSC Ensembl
chr14:85799131..85850007hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3850877
hg1950877
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480382
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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