A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986614



Internal ID58515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102219795..102219843hg38UCSC Ensembl
chr6:102667670..102667718hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5409906
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986614
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00359


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