A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418086



Internal ID21075639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66805335..66810663hg38UCSC Ensembl
chr8:67717570..67722898hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg385329
hg195329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169428
Samples
Known GenesC8orf44-SGK3, SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418086
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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