A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3420115



Internal ID15267073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83187889..83187908hg38UCSC Ensembl
Innerchr15:83187857..83187940hg38UCSC Ensembl
Outerchr15:83187838..83187959hg38UCSC Ensembl
chr15:83856641..83856660hg19UCSC Ensembl
Innerchr15:83856609..83856692hg19UCSC Ensembl
Outerchr15:83856590..83856711hg19UCSC Ensembl
chr15:81647645..81647664hg18UCSC Ensembl
Innerchr15:81647696..81647613hg18UCSC Ensembl
Outerchr15:81647594..81647715hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865832
SamplesNA12005
Known GenesHDGFRP3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3420115
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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