A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455874



Internal ID233947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170307624..170312472hg38UCSC Ensembl
chr6:170616712..170621560hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384849
hg194849
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991331
Samples
Known GenesFAM120B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455874
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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