A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454598



Internal ID232696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111620676..111620854hg38UCSC Ensembl
chr6:111941879..111942057hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454598
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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