A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3366644



Internal ID15213621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98151034..98151053hg38UCSC Ensembl
Innerchr13:98151030..98151057hg38UCSC Ensembl
Outerchr13:98151011..98151076hg38UCSC Ensembl
chr13:98803288..98803307hg19UCSC Ensembl
Innerchr13:98803284..98803311hg19UCSC Ensembl
Outerchr13:98803265..98803330hg19UCSC Ensembl
chr13:97601289..97601308hg18UCSC Ensembl
Innerchr13:97601312..97601285hg18UCSC Ensembl
Outerchr13:97601266..97601331hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9663514, essv9663492, essv9663481, essv9663503
SamplesNA12812, NA11918, NA12815, NA11881
Known GenesFARP1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3366644
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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