A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910417



Internal ID22685628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116579230..116579524hg38UCSC Ensembl
chr8:117591469..117591763hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446655
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910417
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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