A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3449890



Internal ID15296838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22537487..22552585hg38UCSC Ensembl
Innerchr15:22538487..22551585hg38UCSC Ensembl
Outerchr15:22536487..22553585hg38UCSC Ensembl
chr15:23320511..23335609hg19UCSC Ensembl
Innerchr15:23321511..23334609hg19UCSC Ensembl
Outerchr15:23319511..23336609hg19UCSC Ensembl
chr15:20871952..20887050hg18UCSC Ensembl
Innerchr15:20872952..20886050hg18UCSC Ensembl
Outerchr15:20870952..20888050hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3815099
hg1915099
hg1815099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1377e59
Supporting Variantsessv8689681
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3449890
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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