A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933890



Internal ID22709208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49022510..49022570hg38UCSC Ensembl
chr15:49314707..49314767hg19UCSC 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 Variantsnssv17379893
Samples
Known GenesSECISBP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933890
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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