A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8639978



Internal ID15145175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114083953..114083953hg38UCSC Ensembl
Innerchr10:114083952..114083954hg38UCSC Ensembl
Outerchr10:114083913..114083973hg38UCSC Ensembl
chr10:115843712..115843712hg19UCSC Ensembl
Innerchr10:115843711..115843713hg19UCSC Ensembl
Outerchr10:115843672..115843732hg19UCSC Ensembl
chr10:115833702..115833702hg18UCSC Ensembl
Innerchr10:115833703..115833701hg18UCSC Ensembl
Outerchr10:115833662..115833722hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3862
hg1962
hg1862
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3448393
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8639978
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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