A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477547



Internal ID21135100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78782065..78793308hg38UCSC Ensembl
chr14:79248408..79259651hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3811244
hg1911244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187447
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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