A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15705898



Internal ID21378174
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 StatusS
Merged Variantsnsv4391316
Supporting Variants
Samples
Known GenesSECISBP2L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15705898
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0373563


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