A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911609



Internal ID22686824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27084329..27087661hg38UCSC Ensembl
chr8:26941846..26945178hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg383333
hg193333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911609
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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