A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888347



Internal ID22663352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130298769..130320475hg38UCSC Ensembl
chr3:130017612..130039318hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3821707
hg1921707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405089
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888347
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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