A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307615



Internal ID14807877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30977629..30977630hg38UCSC Ensembl
Innerchr15:30977583..30977676hg38UCSC Ensembl
Outerchr15:30977582..30977677hg38UCSC Ensembl
chr15:31269832..31269833hg19UCSC Ensembl
Innerchr15:31269786..31269879hg19UCSC Ensembl
Outerchr15:31269785..31269880hg19UCSC Ensembl
chr15:29057124..29057125hg18UCSC Ensembl
Innerchr15:29057171..29057078hg18UCSC Ensembl
Outerchr15:29057077..29057172hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38211
hg19211
hg18211
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7756169, essv7742286
SamplesNA18870, NA18519
Known GenesMTMR10
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307615
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer