A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229698



Internal ID20796738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34922501..34929300hg38UCSC Ensembl
chr8:34780019..34786818hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229698
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00041


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