A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182103



Internal ID20749143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66277222..66286817hg38UCSC Ensembl
chr15:66569560..66579155hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg389596
hg199596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182103
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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