A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3309600



Internal ID14809865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25937006..25937007hg38UCSC Ensembl
Innerchr10:25936989..25937024hg38UCSC Ensembl
Outerchr10:25936988..25937025hg38UCSC Ensembl
chr10:26225935..26225936hg19UCSC Ensembl
Innerchr10:26225918..26225953hg19UCSC Ensembl
Outerchr10:26225917..26225954hg19UCSC Ensembl
chr10:26265941..26265942hg18UCSC Ensembl
Innerchr10:26265959..26265924hg18UCSC Ensembl
Outerchr10:26265923..26265960hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38261
hg19261
hg18261
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7843071, essv7841004, essv7842773, essv7840065
SamplesNA12891, NA19238, NA19239, NA12878
Known GenesMYO3A
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3309600
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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