A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234706



Internal ID20801746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65429393..65436345hg38UCSC Ensembl
chr8:66341628..66348580hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg386953
hg196953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424121
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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