A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915041



Internal ID22690259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:136280062..136323100hg38UCSC Ensembl
chr8:137292305..137335343hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3843039
hg1943039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915041
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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