A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098137



Internal ID22007370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23305581..23305581hg38UCSC Ensembl
chr16:23316902..23316902hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605490
Samples
Known GenesSCNN1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098137
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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