A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621219



Internal ID7008088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99084600..99098835hg38UCSC Ensembl
chr9:101846882..101861117hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3814236
hg1914236
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13579217, essv13579218, essv13579215, essv13579220, essv13579219, essv13579216
SamplesNA21089, NA20896, NA21144, NA20902, NA20847, HG04161
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621219
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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