A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689768



Internal ID15054995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42154462..42155460hg38UCSC Ensembl
Innerchr15:42154461..42155461hg38UCSC Ensembl
Outerchr15:42153462..42156460hg38UCSC Ensembl
chr15:42446660..42447658hg19UCSC Ensembl
Innerchr15:42446659..42447659hg19UCSC Ensembl
Outerchr15:42445660..42448658hg19UCSC Ensembl
chr15:40233952..40234950hg18UCSC Ensembl
Innerchr15:40234951..40233951hg18UCSC Ensembl
Outerchr15:40232952..40235950hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3446241
Supporting Variants
SamplesNA19239
Known GenesPLA2G4F
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689768
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