A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988840



Internal ID59985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117414150..117423403hg38UCSC Ensembl
chr6:117735313..117744566hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg389254
hg199254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460018
Supporting Variants
Samples
Known GenesROS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988840
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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