A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178574



Internal ID20745614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60542426..60542667hg38UCSC Ensembl
chr15:60834625..60834866hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511046
Supporting Variants
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178574
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00086


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