A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422771



Internal ID21080324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106364901..106366900hg38UCSC Ensembl
chr8:107377129..107379128hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162390
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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