A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905483



Internal ID22680670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196592196..196593196hg38UCSC Ensembl
chr3:196319067..196320067hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905483
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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