A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166051



Internal ID20733091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21238836..21388543hg38UCSC Ensembl
chr8:21096347..21246054hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38149708
hg19149708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417227
Supporting Variants
Samples
Known GenesLOC101929172
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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