A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006182



Internal ID7071275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:25094045..25107990hg38UCSC Ensembl
Outerchr2:25316914..25330859hg19UCSC Ensembl
Outerchr2:25170418..25184363hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3813946
hg1913946
hg1813946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563648
SamplesHuRef
Known GenesEFR3B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006182
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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