A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986811



Internal ID58646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88444928..88454331hg38UCSC Ensembl
chr6:89154647..89164050hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg389404
hg199404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986811
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002499


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