A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272823



Internal ID20482041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69207946..69207946hg38UCSC Ensembl
chr16:69241849..69241849hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759880
Supporting Variants
Samples
Known GenesSNTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272823
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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