A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7836938



Internal ID15038114
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 StatusS
Merged Variantsesv3307902
Supporting Variants
SamplesNA19239
Known GenesAPOL3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7836938
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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