A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006867



Internal ID21916210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128464665..128464862hg38UCSC Ensembl
chr9:131226944..131227141hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586149
Samples
Known GenesODF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006867
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