A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270868



Internal ID20480086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49022508..49022569hg38UCSC Ensembl
chr15:49314705..49314766hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739670
Supporting Variants
Samples
Known GenesSECISBP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270868
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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