A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887563



Internal ID22662555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39644011..39648085hg38UCSC Ensembl
chr3:39685502..39689576hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg384075
hg194075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887563
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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