A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014681



Internal ID21924024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6486632..6486700hg38UCSC Ensembl
chr9:6486632..6486700hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578558
Samples
Known GenesUHRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014681
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