A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908036



Internal ID22683246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110837334..110852573hg38UCSC Ensembl
chr8:111849563..111864802hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3815240
hg1915240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446947
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908036
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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