A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419666



Internal ID22477536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23597793..23599032hg38UCSC Ensembl
chr3:23639284..23640523hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5902649
Supporting Variants
Samples
Known GenesMIR548AC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419666
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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