A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191286



Internal ID20758326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90245215..90246012hg38UCSC Ensembl
chr15:90788447..90789244hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498784
Supporting Variants
Samples
Known GenesCIB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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