A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857060



Internal ID22631995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79332883..79335132hg38UCSC Ensembl
chr14:79799226..79801475hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg382250
hg192250
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466823, nssv17461442
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857060
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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