A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3374358



Internal ID15221333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36958965..36959280hg38UCSC Ensembl
Innerchr22:36958965..36959280hg38UCSC Ensembl
Outerchr22:36958698..36960488hg38UCSC Ensembl
chr22:37355006..37355321hg19UCSC Ensembl
Innerchr22:37355006..37355321hg19UCSC Ensembl
Outerchr22:37354739..37356529hg19UCSC Ensembl
chr22:35684952..35685267hg18UCSC Ensembl
Innerchr22:35684952..35685267hg18UCSC Ensembl
Outerchr22:35684685..35686475hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38316
hg19316
hg18316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652163
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3374358
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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