A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3305817



Internal ID15152765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33880946..33880947hg38UCSC Ensembl
Innerchr3:33880904..33880989hg38UCSC Ensembl
Outerchr3:33880903..33880990hg38UCSC Ensembl
chr3:33922438..33922439hg19UCSC Ensembl
Innerchr3:33922396..33922481hg19UCSC Ensembl
Outerchr3:33922395..33922482hg19UCSC Ensembl
chr3:33897442..33897443hg18UCSC Ensembl
Innerchr3:33897485..33897400hg18UCSC Ensembl
Outerchr3:33897399..33897486hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381354
hg191354
hg181354
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7758208, essv7745387, essv7750423
SamplesNA19257, NA19147, NA18522
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3305817
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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