A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8968586



Internal ID14872185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60700560..60700603hg38UCSC Ensembl
Innerchr15:60700578..60700585hg38UCSC Ensembl
Outerchr15:60700542..60700621hg38UCSC Ensembl
chr15:60992759..60992802hg19UCSC Ensembl
Innerchr15:60992777..60992784hg19UCSC Ensembl
Outerchr15:60992741..60992820hg19UCSC Ensembl
chr15:58780051..58780094hg18UCSC Ensembl
Innerchr15:58780069..58780076hg18UCSC Ensembl
Outerchr15:58780033..58780112hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38155
hg19155
hg18155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3426459
Supporting Variants
SamplesNA19116
Known GenesRORA
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8968586
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