A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740827



Internal ID15083982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74512556..74512556hg38UCSC Ensembl
Innerchr15:74512555..74512557hg38UCSC Ensembl
Outerchr15:74512506..74512606hg38UCSC Ensembl
chr15:74804897..74804897hg19UCSC Ensembl
Innerchr15:74804896..74804898hg19UCSC Ensembl
Outerchr15:74804847..74804947hg19UCSC Ensembl
chr15:72591950..72591950hg18UCSC Ensembl
Innerchr15:72591951..72591949hg18UCSC Ensembl
Outerchr15:72591900..72592000hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38306
hg19306
hg18306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3395488
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740827
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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