A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487090



Internal ID264437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36257643..36267471hg38UCSC Ensembl
chr9:36257640..36267468hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg389829
hg199829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023708
Samples
Known GenesGNE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487090
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