A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621479



Internal ID6661658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111000061..111012393hg38UCSC Ensembl
Innerchr9:111000061..111012393hg38UCSC Ensembl
Outerchr9:110999561..111012893hg38UCSC Ensembl
chr9:113762341..113774673hg19UCSC Ensembl
Innerchr9:113762341..113774673hg19UCSC Ensembl
Outerchr9:113761841..113775173hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3812333
hg1912333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13601055
SamplesHG04107
Known GenesLPAR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621479
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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