A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166059



Internal ID20733099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21309001..21317600hg38UCSC Ensembl
chr8:21166512..21175111hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418818
Supporting Variants
Samples
Known GenesLOC101929172
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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