A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3366896



Internal ID15213872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38188968..38189308hg38UCSC Ensembl
Innerchr22:38188968..38189308hg38UCSC Ensembl
Outerchr22:38188490..38189579hg38UCSC Ensembl
chr22:38584975..38585315hg19UCSC Ensembl
Innerchr22:38584975..38585315hg19UCSC Ensembl
Outerchr22:38584497..38585586hg19UCSC Ensembl
chr22:36914921..36915261hg18UCSC Ensembl
Innerchr22:36914921..36915261hg18UCSC Ensembl
Outerchr22:36914443..36915532hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38341
hg19341
hg18341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652165
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3366896
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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