A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621426



Internal ID6661605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109008152..109008911hg38UCSC Ensembl
Innerchr9:109008158..109008905hg38UCSC Ensembl
Outerchr9:109008146..109008917hg38UCSC Ensembl
chr9:111770432..111771191hg19UCSC Ensembl
Innerchr9:111770438..111771185hg19UCSC Ensembl
Outerchr9:111770426..111771197hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13595218, essv13595219, essv13595220
SamplesNA19429, NA19700, NA18615
Known GenesCTNNAL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621426
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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