A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987960



Internal ID59406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110350507..110350532hg38UCSC Ensembl
chr6:110671710..110671735hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546502
Supporting Variants
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987960
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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