A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3389714



Internal ID15236681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121147799..121147799hg38UCSC Ensembl
Innerchr10:121147798..121147800hg38UCSC Ensembl
Outerchr10:121147749..121147849hg38UCSC Ensembl
chr10:122907313..122907313hg19UCSC Ensembl
Innerchr10:122907312..122907314hg19UCSC Ensembl
Outerchr10:122907263..122907363hg19UCSC Ensembl
chr10:122897303..122897303hg18UCSC Ensembl
Innerchr10:122897304..122897302hg18UCSC Ensembl
Outerchr10:122897253..122897353hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3882
hg1982
hg1882
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8653022, essv8653021, essv8653020
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3389714
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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