A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899453



Internal ID22674583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:132232484..132370921hg38UCSC Ensembl
chr4:133153639..133292076hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38138438
hg19138438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422744
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899453
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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