A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621045



Internal ID7007915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90410378..90412750hg38UCSC Ensembl
Innerchr9:90410379..90412749hg38UCSC Ensembl
Outerchr9:90410377..90412751hg38UCSC Ensembl
chr9:93172660..93175032hg19UCSC Ensembl
Innerchr9:93172661..93175031hg19UCSC Ensembl
Outerchr9:93172659..93175033hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382373
hg192373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13554004, essv13554006, essv13554005, essv13554003
SamplesHG00346, HG00326, HG00188, NA11832
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621045
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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