A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3432140



Internal ID15279096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17769003..17858466hg38UCSC Ensembl
Innerchr12:17770993..17856886hg38UCSC Ensembl
Outerchr12:17768893..17858586hg38UCSC Ensembl
chr12:17921937..18011400hg19UCSC Ensembl
Innerchr12:17923927..18009820hg19UCSC Ensembl
Outerchr12:17921827..18011520hg19UCSC Ensembl
chr12:17813204..17902667hg18UCSC Ensembl
Innerchr12:17815194..17901087hg18UCSC Ensembl
Outerchr12:17813094..17902787hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3889464
hg1989464
hg1889464
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8808614
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3432140
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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