A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916084



Internal ID22691303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8404325..8505437hg38UCSC Ensembl
chr8:8261835..8362947hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38101113
hg19101113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916084
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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