A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426668



Internal ID22484538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30490460..30490460hg38UCSC Ensembl
chr3:30531952..30531952hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426668
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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