A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166357



Internal ID20733397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1793559..1917954hg38UCSC Ensembl
chr8:1741725..1866120hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38124396
hg19124396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432261
Supporting Variants
Samples
Known GenesARHGEF10, MIR596
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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