A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3353214



Internal ID14853478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30977617..30977659hg38UCSC Ensembl
Innerchr15:30977633..30977641hg38UCSC Ensembl
Outerchr15:30977599..30977677hg38UCSC Ensembl
chr15:31269820..31269862hg19UCSC Ensembl
Innerchr15:31269836..31269844hg19UCSC Ensembl
Outerchr15:31269802..31269880hg19UCSC Ensembl
chr15:29057112..29057154hg18UCSC Ensembl
Innerchr15:29057128..29057136hg18UCSC Ensembl
Outerchr15:29057094..29057172hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38115
hg19115
hg18115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8967686, essv8967687
SamplesNA18870, NA18519
Known GenesMTMR10
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3353214
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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