A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901406



Internal ID22676556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35784357..35837624hg38UCSC Ensembl
chr4:35785979..35839246hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3853268
hg1953268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901406
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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