A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3333628



Internal ID15180615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78874585..78874603hg38UCSC Ensembl
Innerchr15:78874555..78874633hg38UCSC Ensembl
Outerchr15:78874537..78874651hg38UCSC Ensembl
chr15:79166927..79166945hg19UCSC Ensembl
Innerchr15:79166897..79166975hg19UCSC Ensembl
Outerchr15:79166879..79166993hg19UCSC Ensembl
chr15:76953982..76954000hg18UCSC Ensembl
Innerchr15:76954030..76953952hg18UCSC Ensembl
Outerchr15:76953934..76954048hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865828
SamplesNA18522
Known GenesMORF4L1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3333628
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer