A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923726



Internal ID22698953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8460175..8593159hg38UCSC Ensembl
chr8:8317685..8450669hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38132985
hg19132985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1984n209
Supporting Variantsnssv17446021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923726
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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