A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416042



Internal ID22473912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172590031..172600320hg38UCSC Ensembl
chr3:172307821..172318110hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3810290
hg1910290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907285
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416042
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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