A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854644



Internal ID22629579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47657759..47660311hg38UCSC Ensembl
chr15:47949956..47952508hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg382553
hg192553
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471918
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854644
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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