A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595317



Internal ID21787360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79386106..79391264hg38UCSC Ensembl
chr8:80298341..80303499hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385159
hg195159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016583
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595317
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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