A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17410616



Internal ID22468486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31525165..31530293hg38UCSC Ensembl
chr3:31566657..31571785hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg385129
hg195129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900208
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17410616
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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