A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020973



Internal ID20588013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79556540..79558690hg38UCSC Ensembl
chr14:80022883..80025033hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg382151
hg192151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485952
Supporting Variants
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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