A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231455



Internal ID20798495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9653501..9657200hg38UCSC Ensembl
chr8:9511011..9514710hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416850
Supporting Variants
Samples
Known GenesTNKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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