A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006150



Internal ID21915493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66129159..66144583hg38UCSC Ensembl
chr9:42376683..42392103hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3815425
hg1915421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580855
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006150
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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