A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020959



Internal ID20587999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79281022..79281584hg38UCSC Ensembl
chr14:79747365..79747927hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491680
Supporting Variants
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020959
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00014


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