A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391316



Internal ID21382346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49022511..49022571hg38UCSC Ensembl
chr15:49314708..49314768hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705898
Samples
Known GenesSECISBP2L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391316
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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