A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192455



Internal ID20759496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43385667..43393682hg38UCSC Ensembl
chr15:43677865..43685880hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg388016
hg198016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508302
Supporting Variants
Samples
Known GenesRNU6-28P, TUBGCP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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