A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416565



Internal ID22474435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39575788..39575788hg38UCSC Ensembl
chr3:39617279..39617279hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961691
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416565
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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