A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890787



Internal ID22665816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193721259..193725592hg38UCSC Ensembl
chr3:193439048..193443381hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg384334
hg194334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890787
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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