A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898511



Internal ID22673627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39179581..39183057hg38UCSC Ensembl
chr5:39179683..39183159hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg383477
hg193477
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414062
Samples
Known GenesFYB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898511
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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