A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455961



Internal ID234029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116903437..116904143hg38UCSC Ensembl
chr6:117224600..117225306hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987485
Samples
Known GenesRFX6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455961
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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