A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890430



Internal ID22665458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12887563..12887997hg38UCSC Ensembl
chr4:12889187..12889621hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890430
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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