A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3385002



Internal ID15231972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46578473..46585171hg38UCSC Ensembl
Innerchr10:46579473..46584171hg38UCSC Ensembl
Outerchr10:46577473..46586171hg38UCSC Ensembl
chr10:46964446..46971144hg19UCSC Ensembl
Innerchr10:46965446..46970144hg19UCSC Ensembl
Outerchr10:46963446..46972144hg19UCSC Ensembl
chr10:46384452..46391150hg18UCSC Ensembl
Innerchr10:46385452..46390150hg18UCSC Ensembl
Outerchr10:46383452..46392150hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg386699
hg196699
hg186699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv410e59
Supporting Variantsessv8688065
SamplesNA12878
Known GenesSYT15
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3385002
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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