A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432076



Internal ID22489946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12474780..12525091hg38UCSC Ensembl
chr7:12514406..12564717hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3850312
hg1950312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909381
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432076
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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