A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467309



Internal ID22525200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78361074..78363441hg38UCSC Ensembl
chr14:78827417..78829784hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382368
hg192368
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857343
Supporting Variants
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467309
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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