A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8967879



Internal ID13244348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37415675..37415689hg38UCSC Ensembl
Innerchr15:37415666..37415696hg38UCSC Ensembl
Outerchr15:37415652..37415710hg38UCSC Ensembl
chr15:37707876..37707890hg19UCSC Ensembl
Innerchr15:37707867..37707897hg19UCSC Ensembl
Outerchr15:37707853..37707911hg19UCSC Ensembl
chr15:35495168..35495182hg18UCSC Ensembl
Innerchr15:35495189..35495159hg18UCSC Ensembl
Outerchr15:35495145..35495203hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38663
hg19663
hg18663
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3423841
Supporting Variants
SamplesNA11993
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8967879
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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