A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422096



Internal ID22479966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30295280..30295280hg38UCSC Ensembl
chr3:30336771..30336771hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5953726
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422096
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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