A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3447239



Internal ID15294189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88860440..90208808hg38UCSC Ensembl
Innerchr2:88862430..90207228hg38UCSC Ensembl
Outerchr2:88860330..90208928hg38UCSC Ensembl
chr2:89159952..90247674hg19UCSC Ensembl
Innerchr2:89161942..90246094hg19UCSC Ensembl
Outerchr2:89159842..90247794hg19UCSC Ensembl
chr2:88941067..89884979hg18UCSC Ensembl
Innerchr2:88943057..89883399hg18UCSC Ensembl
Outerchr2:88940957..89885099hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381348369
hg191087723
hg18943913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8809127
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3447239
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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