A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412088



Internal ID22469958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24512034..24512034hg38UCSC Ensembl
chr3:24553525..24553525hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412088
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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