A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988837



Internal ID59983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117361456..117361496hg38UCSC Ensembl
chr6:117682619..117682659hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546994
Supporting Variants
Samples
Known GenesROS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988837
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00281


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