A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407852



Internal ID22465722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145814698..145815750hg38UCSC Ensembl
chr3:145532485..145533537hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381053
hg191053
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407852
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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