A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285484



Internal ID20494702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28322899..28322968hg38UCSC Ensembl
chr16:28334220..28334289hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743285
Supporting Variants
Samples
Known GenesSBK1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285484
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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