A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3386766



Internal ID14887048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13061801..13063254hg38UCSC Ensembl
Innerchr10:13061800..13063255hg38UCSC Ensembl
Outerchr10:13061691..13063374hg38UCSC Ensembl
chr10:13103801..13105254hg19UCSC Ensembl
Innerchr10:13103800..13105255hg19UCSC Ensembl
Outerchr10:13103691..13105374hg19UCSC Ensembl
chr10:13143807..13145260hg18UCSC Ensembl
Innerchr10:13145261..13143806hg18UCSC Ensembl
Outerchr10:13143697..13145380hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381454
hg191454
hg181454
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808490
SamplesNA12878
Known GenesCCDC3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3386766
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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