A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895390



Internal ID22670472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31501820..31520268hg38UCSC Ensembl
chr3:31543312..31561760hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3818449
hg1918449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413057
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895390
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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