A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379893



Internal ID22437763
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 StatusS
Merged Variantsnsv5933890
Supporting Variants
Samples
Known GenesSECISBP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379893
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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