A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490361



Internal ID21147914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77416001..77418400hg38UCSC Ensembl
chr14:77882344..77884743hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189897
Samples
Known GenesNOXRED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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