A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621190



Internal ID6661369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97570964..97628055hg38UCSC Ensembl
chr9:100333246..100390337hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3857092
hg1957092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13573676
SamplesHG04152
Known GenesTMOD1, TSTD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621190
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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