A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919697



Internal ID22694919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:46863139..46863459hg38UCSC Ensembl
chr8:47774761..47775081hg19UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919697
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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