A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3426459



Internal ID15273416
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 StatusM
Merged Variants
Supporting Variantsessv8968585, essv8968586, essv8968584
SamplesNA19102, NA19116, NA18965
Known GenesRORA
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3426459
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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