A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900043



Internal ID22675181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108990444..109014111hg38UCSC Ensembl
chr5:108326145..108349812hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3823668
hg1923668
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416454
Samples
Known GenesFER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900043
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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