A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866171



Internal ID22641106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78890630..78902883hg38UCSC Ensembl
chr14:79356973..79369226hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3812254
hg1912254
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456955
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866171
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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