A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8689562



Internal ID15019647
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 StatusS
Merged Variantsesv3378621
Supporting Variants
SamplesNA19238
Known GenesHERC2P3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8689562
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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