A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621810



Internal ID6661986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128464113..128473904hg38UCSC Ensembl
Innerchr9:128464263..128473754hg38UCSC Ensembl
Outerchr9:128463963..128474054hg38UCSC Ensembl
chr9:131226392..131236183hg19UCSC Ensembl
Innerchr9:131226542..131236033hg19UCSC Ensembl
Outerchr9:131226242..131236333hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg389792
hg199792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13622831, essv13622830
SamplesNA20891, NA20864
Known GenesODF2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621810
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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