A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477080



Internal ID21134633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78765400..78774047hg38UCSC Ensembl
chr14:79231743..79240390hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg388648
hg198648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181799
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477080
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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