A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092862



Internal ID21462212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78692800..78699299hg38UCSC Ensembl
chr14:79159143..79165642hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603567
Supporting Variants
SamplesHG02818
Known GenesNRXN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092862
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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