A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563994



Internal ID336918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34109636..34120544hg38UCSC Ensembl
chr6:34077413..34088321hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3810909
hg1910909
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982028
Samples
Known GenesGRM4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563994
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