A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621249



Internal ID6661428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101368883..101371369hg38UCSC Ensembl
Innerchr9:101368883..101371369hg38UCSC Ensembl
Outerchr9:101368604..101371691hg38UCSC Ensembl
chr9:104131165..104133651hg19UCSC Ensembl
Innerchr9:104131165..104133651hg19UCSC Ensembl
Outerchr9:104130886..104133973hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg382487
hg192487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13581739
SamplesHG01809
Known GenesBAAT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621249
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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