A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229462



Internal ID20796502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15805107..16097298hg38UCSC Ensembl
chr8:15662616..15954807hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38292192
hg19292192
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229462
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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