A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893347



Internal ID22668406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164331283..164420703hg38UCSC Ensembl
chr3:164049071..164138491hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3889421
hg1989421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893347
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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