A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191189



Internal ID20758229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68195987..68196339hg38UCSC Ensembl
chr15:68488325..68488677hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507803
Supporting Variants
Samples
Known GenesCALML4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191189
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00016


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