A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3412267



Internal ID14912540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129518310..129518892hg38UCSC Ensembl
Innerchr10:129518310..129518892hg38UCSC Ensembl
Outerchr10:129517885..129519456hg38UCSC Ensembl
chr10:131316574..131317156hg19UCSC Ensembl
Innerchr10:131316574..131317156hg19UCSC Ensembl
Outerchr10:131316149..131317720hg19UCSC Ensembl
chr10:131206564..131207146hg18UCSC Ensembl
Innerchr10:131206564..131207146hg18UCSC Ensembl
Outerchr10:131206139..131207710hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38583
hg19583
hg18583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8651773
SamplesNA19240
Known GenesMGMT
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3412267
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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