A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191587



Internal ID20758627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59091435..59133296hg38UCSC Ensembl
chr15:59383634..59425495hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3841862
hg1941862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504260
Supporting Variants
Samples
Known GenesCCNB2, RNF111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191587
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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