A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169366



Internal ID20736406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65780115..66156141hg38UCSC Ensembl
chr8:66692350..67068376hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38376027
hg19376027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433460
Supporting Variants
Samples
Known GenesDNAJC5B, PDE7A, TRIM55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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