A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900105



Internal ID22675244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158316636..158316796hg38UCSC Ensembl
chr4:159237788..159237948hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900105
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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