A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890052



Internal ID22665077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43378023..43378100hg38UCSC Ensembl
chr5:43378125..43378202hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890052
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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