A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910858



Internal ID22686070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106523406..106536260hg38UCSC Ensembl
chr8:107535634..107548488hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3812855
hg1912855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430881
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910858
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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