A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557026



Internal ID330143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78626750..78627208hg38UCSC Ensembl
chr14:79093093..79093551hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699434
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557026
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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