A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481866



Internal ID259332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92413442..92647793hg38UCSC Ensembl
chr9:95175724..95410075hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38234352
hg19234352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027412
Samples
Known GenesASPN, CENPP, ECM2, IPPK, LOC100128361, MIR4670, OMD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481866
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