A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5404805



Internal ID184151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117301286..117301337hg38UCSC Ensembl
chr6:117622449..117622500hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735609
Samples
Known GenesROS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5404805
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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