A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484219



Internal ID21141772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51984001..51992400hg38UCSC Ensembl
chr14:52450719..52459118hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190553
Samples
Known GenesC14orf166
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484219
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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