A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8811050



Internal ID15107767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123904877..123904877hg38UCSC Ensembl
Innerchr10:123904876..123904878hg38UCSC Ensembl
Outerchr10:123904817..123904927hg38UCSC Ensembl
chr10:125664393..125664393hg19UCSC Ensembl
Innerchr10:125664392..125664394hg19UCSC Ensembl
Outerchr10:125664333..125664443hg19UCSC Ensembl
chr10:125654383..125654383hg18UCSC Ensembl
Innerchr10:125654384..125654382hg18UCSC Ensembl
Outerchr10:125654323..125654433hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3860
hg1960
hg1860
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3345467
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8811050
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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