A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182094



Internal ID20749134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45440648..45442329hg38UCSC Ensembl
chr15:45732846..45734527hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381682
hg191682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182094
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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