A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7841726



Internal ID15083185
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 StatusS
Merged Variantsesv3308789
Supporting Variants
SamplesNA19240
Known GenesHOMER2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7841726
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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