A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3347632



Internal ID15194614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20435585..20447483hg38UCSC Ensembl
Innerchr15:20436585..20446483hg38UCSC Ensembl
Outerchr15:20434585..20448483hg38UCSC Ensembl
chr15:20640838..20652736hg19UCSC Ensembl
Innerchr15:20641838..20651736hg19UCSC Ensembl
Outerchr15:20639838..20653736hg19UCSC Ensembl
chr15:18900852..18912750hg18UCSC Ensembl
Innerchr15:18901852..18911750hg18UCSC Ensembl
Outerchr15:18899852..18913750hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3811899
hg1911899
hg1811899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1356e59
Supporting Variantsessv8689556
SamplesNA19239
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3347632
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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