A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903384



Internal ID22678551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127431774..127438776hg38UCSC Ensembl
chr3:127150617..127157619hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg387003
hg197003
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903384
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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