A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8642059



Internal ID14802097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68409477..68409477hg38UCSC Ensembl
Innerchr15:68409476..68409478hg38UCSC Ensembl
Outerchr15:68409437..68409497hg38UCSC Ensembl
chr15:68701816..68701816hg19UCSC Ensembl
Innerchr15:68701815..68701817hg19UCSC Ensembl
Outerchr15:68701776..68701836hg19UCSC Ensembl
chr15:66488870..66488870hg18UCSC Ensembl
Innerchr15:66488871..66488869hg18UCSC Ensembl
Outerchr15:66488830..66488890hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3401926
Supporting Variants
Samples
Known GenesITGA11
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8642059
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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