A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018800



Internal ID21928143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127980551..127980685hg38UCSC Ensembl
chr9:130742830..130742964hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018800
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