A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903137



Internal ID22678301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:19568918..19568993hg38UCSC Ensembl
chr4:19570541..19570616hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903137
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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