A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7754934



Internal ID13915215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36165249..36165250hg38UCSC Ensembl
Innerchr22:36165223..36165276hg38UCSC Ensembl
Outerchr22:36165222..36165277hg38UCSC Ensembl
chr22:36561297..36561298hg19UCSC Ensembl
Innerchr22:36561271..36561324hg19UCSC Ensembl
Outerchr22:36561270..36561325hg19UCSC Ensembl
chr22:34891243..34891244hg18UCSC Ensembl
Innerchr22:34891270..34891217hg18UCSC Ensembl
Outerchr22:34891216..34891271hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38162
hg19162
hg18162
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307709
Supporting Variants
SamplesNA18523
Known GenesAPOL3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7754934
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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