A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565684



Internal ID7037066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:13975134..14070720hg38UCSC Ensembl
Outerchr21:15347455..15443041hg19UCSC Ensembl
Outerchr21:14269326..14364912hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3895587
hg1995587
hg1895587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005089
Supporting Variants
SamplesHuRef
Known GenesANKRD20A11P
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565684
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