A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002005



Internal ID21911348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15002290..15003099hg38UCSC Ensembl
chr9:15002288..15003097hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587712
Samples
Known GenesLOC389705
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002005
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