A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420370



Internal ID22478240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180899485..180899485hg38UCSC Ensembl
chr3:180617273..180617273hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5955187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420370
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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