A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033765



Internal ID20600805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89509301..89543900hg38UCSC Ensembl
chr16:89575709..89610308hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3834600
hg1934600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507857
Supporting Variants
Samples
Known GenesSPG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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