A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476022



Internal ID21133575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79841755..79877569hg38UCSC Ensembl
chr14:80308098..80343912hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3835815
hg1935815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187764
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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