A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894097



Internal ID22669166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40101278..40101509hg38UCSC Ensembl
chr5:40101380..40101611hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894097
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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