A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191244



Internal ID20758284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68918701..68989100hg38UCSC Ensembl
chr15:69211040..69281439hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3870400
hg1970400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502545
Supporting Variants
Samples
Known GenesMIR548H4, NOX5, SPESP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191244
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00036


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