A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023390



Internal ID20590430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35389908..35393951hg38UCSC Ensembl
chr15:35682109..35686152hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384044
hg194044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514838
Supporting Variants
Samples
Known GenesDPH6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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