A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986372



Internal ID58345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109319888..109319962hg38UCSC Ensembl
chr6:109641091..109641165hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986372
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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