A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696672



Internal ID21218522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98825716..98825795hg38UCSC Ensembl
chr8:99837944..99838023hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818206
Supporting Variants
Samples
Known GenesSTK3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696672
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.673077


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