A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563233



Internal ID336170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20656599..20935008hg38UCSC Ensembl
chr6:20656830..20935239hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38278410
hg19278410
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981247
Samples
Known GenesCDKAL1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563233
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer