A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097041



Internal ID22006274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18507476..18507476hg38UCSC Ensembl
chr16:14982406..14982406hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616121
Samples
Known GenesNOMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097041
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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