A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13573676



Internal ID3575492
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621190
Supporting Variants
SamplesHG04152
Known GenesTMOD1, TSTD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13573676
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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