A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466193



Internal ID244038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110132984..110136022hg38UCSC Ensembl
chr6:110454187..110457225hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383039
hg193039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987938
Samples
Known GenesWASF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466193
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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