A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8967687



Internal ID14042421
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 StatusS
Merged Variantsesv3353214
Supporting Variants
SamplesNA18870
Known GenesMTMR10
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8967687
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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