A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307902



Internal ID15154850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36165222..36165223hg38UCSC Ensembl
Innerchr22:36165177..36165268hg38UCSC Ensembl
Outerchr22:36165176..36165269hg38UCSC Ensembl
chr22:36561270..36561271hg19UCSC Ensembl
Innerchr22:36561225..36561316hg19UCSC Ensembl
Outerchr22:36561224..36561317hg19UCSC Ensembl
chr22:34891216..34891217hg18UCSC Ensembl
Innerchr22:34891262..34891171hg18UCSC Ensembl
Outerchr22:34891170..34891263hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38115
hg19115
hg18115
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7837305, essv7836938, essv7838400
SamplesNA12891, NA19239, NA19240
Known GenesAPOL3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307902
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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