A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169058



Internal ID20736098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54434922..54439730hg38UCSC Ensembl
chr8:55347482..55352290hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg384809
hg194809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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