A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166312



Internal ID20733352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17418789..17495612hg38UCSC Ensembl
chr8:17276298..17353121hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3876824
hg1976824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166312
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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