A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986752



Internal ID58608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111800492..111800542hg38UCSC Ensembl
chr6:112121695..112121745hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382235
hg192235
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563916
Supporting Variants
Samples
Known GenesFYN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986752
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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