A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3344745



Internal ID15191729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28311011..28312709hg38UCSC Ensembl
Innerchr15:28311709..28312011hg38UCSC Ensembl
Outerchr15:28310011..28313709hg38UCSC Ensembl
chr15:28556157..28557855hg19UCSC Ensembl
Innerchr15:28556855..28557157hg19UCSC Ensembl
Outerchr15:28555157..28558855hg19UCSC Ensembl
chr15:26229752..26231450hg18UCSC Ensembl
Innerchr15:26230752..26230450hg18UCSC Ensembl
Outerchr15:26228752..26232450hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1391e59
Supporting Variantsessv8689722
SamplesNA19240
Known GenesHERC2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3344745
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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