A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020918



Internal ID20587958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78745729..78748696hg38UCSC Ensembl
chr14:79212072..79215039hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382968
hg192968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480102
Supporting Variants
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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