A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3358854



Internal ID14859116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121777469..121777485hg38UCSC Ensembl
Innerchr10:121777467..121777485hg38UCSC Ensembl
Outerchr10:121777451..121777503hg38UCSC Ensembl
chr10:123536984..123537000hg19UCSC Ensembl
Innerchr10:123536982..123537000hg19UCSC Ensembl
Outerchr10:123536966..123537018hg19UCSC Ensembl
chr10:123526974..123526990hg18UCSC Ensembl
Innerchr10:123526990..123526972hg18UCSC Ensembl
Outerchr10:123526956..123527008hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8950820, essv8950825, essv8950826, essv8950821, essv8950823, essv8950822
SamplesNA18498, NA18516, NA19099, NA18517, NA18501, NA19129
Known GenesATE1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3358854
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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