A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563604



Internal ID6688646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:46611478..46628407hg38UCSC Ensembl
Outerchr11:46633028..46649957hg19UCSC Ensembl
Outerchr11:46589604..46606533hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3816930
hg1916930
hg1816930
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv993220
Supporting Variants
SamplesHuRef
Known GenesATG13, HARBI1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563604
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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