A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233382



Internal ID20800422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34730248..35150485hg38UCSC Ensembl
chr8:34587766..35008003hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38420238
hg19420238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233382
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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