A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485224



Internal ID262620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6865907..6877296hg38UCSC Ensembl
chr9:6865907..6877296hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3811390
hg1911390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17018984
Samples
Known GenesKDM4C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485224
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