A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3397858



Internal ID15244821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122804279..122804298hg38UCSC Ensembl
Innerchr10:122804275..122804302hg38UCSC Ensembl
Outerchr10:122804256..122804321hg38UCSC Ensembl
chr10:124563795..124563814hg19UCSC Ensembl
Innerchr10:124563791..124563818hg19UCSC Ensembl
Outerchr10:124563772..124563837hg19UCSC Ensembl
chr10:124553785..124553804hg18UCSC Ensembl
Innerchr10:124553808..124553781hg18UCSC Ensembl
Outerchr10:124553762..124553827hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9649980, essv9649991, essv9650003
SamplesNA12814, NA12812, NA18970
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3397858
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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