A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3362497



Internal ID15209475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28015783..28015817hg38UCSC Ensembl
Innerchr10:28015797..28015801hg38UCSC Ensembl
Outerchr10:28015769..28015831hg38UCSC Ensembl
chr10:28304712..28304746hg19UCSC Ensembl
Innerchr10:28304726..28304730hg19UCSC Ensembl
Outerchr10:28304698..28304760hg19UCSC Ensembl
chr10:28344718..28344752hg18UCSC Ensembl
Innerchr10:28344732..28344736hg18UCSC Ensembl
Outerchr10:28344704..28344766hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38253
hg19253
hg18253
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8671774
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3362497
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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