A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3378621



Internal ID15225594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20465385..20475583hg38UCSC Ensembl
Innerchr15:20466385..20474583hg38UCSC Ensembl
Outerchr15:20464385..20476583hg38UCSC Ensembl
chr15:20670638..20680836hg19UCSC Ensembl
Innerchr15:20671638..20679836hg19UCSC Ensembl
Outerchr15:20669638..20681836hg19UCSC Ensembl
chr15:18930652..18940850hg18UCSC Ensembl
Innerchr15:18931652..18939850hg18UCSC Ensembl
Outerchr15:18929652..18941850hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3810199
hg1910199
hg1810199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689562
SamplesNA19238
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3378621
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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