A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743074



Internal ID20519060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166783824..166784395hg38UCSC Ensembl
chr6:167197312..167197883hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296288
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743074
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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