A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3443704



Internal ID15290657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22569687..22571085hg38UCSC Ensembl
Innerchr15:22570085..22570687hg38UCSC Ensembl
Outerchr15:22568687..22572085hg38UCSC Ensembl
chr15:23302011..23303409hg19UCSC Ensembl
Innerchr15:23302409..23303011hg19UCSC Ensembl
Outerchr15:23301011..23304409hg19UCSC Ensembl
chr15:20853452..20854850hg18UCSC Ensembl
Innerchr15:20854452..20853850hg18UCSC Ensembl
Outerchr15:20852452..20855850hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689672
SamplesNA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3443704
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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