A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550206



Internal ID21874561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24512034..24512034hg38UCSC Ensembl
chr3:24553525..24553525hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053345
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550206
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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