A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759880



Internal ID20535740
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 StatusM
Merged Variants
Supporting Variantsnssv16272823
Samples
Known GenesSNTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759880
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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