A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433460



Internal ID21091013
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 StatusM
Merged Variants
Supporting Variantsnssv18169366
Samples
Known GenesDNAJC5B, PDE7A, TRIM55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433460
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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