A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209309



Internal ID20776349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47544624..47548646hg38UCSC Ensembl
chr3:47586114..47590136hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384023
hg194023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370968
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209309
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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