A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182050



Internal ID20749090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26764301..26786300hg38UCSC Ensembl
chr15:27009448..27031447hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3822000
hg1922000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508789
Supporting Variants
Samples
Known GenesGABRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182050
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00056


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