A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689559



Internal ID15094046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20448585..20480383hg38UCSC Ensembl
Innerchr15:20449585..20479383hg38UCSC Ensembl
Outerchr15:20447585..20481383hg38UCSC Ensembl
chr15:20653838..20685636hg19UCSC Ensembl
Innerchr15:20654838..20684636hg19UCSC Ensembl
Outerchr15:20652838..20686636hg19UCSC Ensembl
chr15:18913852..18945650hg18UCSC Ensembl
Innerchr15:18914852..18944650hg18UCSC Ensembl
Outerchr15:18912852..18946650hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3831799
hg1931799
hg1831799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3395014
Supporting Variants
SamplesNA19240
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689559
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