A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991505



Internal ID7061816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:46363996..46382022hg38UCSC Ensembl
Outerchr21:47783911..47801937hg19UCSC Ensembl
Outerchr21:46608339..46626365hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3818027
hg1918027
hg1818027
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563608
SamplesHuRef
Known GenesPCNT
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991505
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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