A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490900



Internal ID21148453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79618301..79650300hg38UCSC Ensembl
chr14:80084644..80116643hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3832000
hg1932000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178338
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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