A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7738383



Internal ID14042560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58484324..58485392hg38UCSC Ensembl
Outerchr15:58484124..58485592hg38UCSC Ensembl
Innerchr15:58776523..58777591hg19UCSC Ensembl
Outerchr15:58776323..58777791hg19UCSC Ensembl
Innerchr15:56563815..56564883hg18UCSC Ensembl
Outerchr15:56563615..56565083hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381469
hg191469
hg181469
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302978
Supporting Variants
SamplesNA18555
Known GenesLIPC
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7738383
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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