A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3308789



Internal ID15155738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82882874..82882875hg38UCSC Ensembl
Innerchr15:82882858..82882883hg38UCSC Ensembl
Outerchr15:82882857..82882883hg38UCSC Ensembl
chr15:83551626..83551627hg19UCSC Ensembl
Innerchr15:83551610..83557693hg19UCSC Ensembl
Outerchr15:83551609..83557694hg19UCSC Ensembl
chr15:81348680..81348681hg18UCSC Ensembl
Innerchr15:81348697..81348664hg18UCSC Ensembl
Outerchr15:81348663..81348698hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386036
hg196036
hg186036
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7843000, essv7841397, essv7841726
SamplesNA19239, NA12892, NA19240
Known GenesHOMER2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3308789
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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