A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990682



Internal ID7076813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:44688138..44708628hg38UCSC Ensembl
Outerchr3:44729630..44750120hg19UCSC Ensembl
Outerchr3:44704634..44725124hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3820491
hg1920491
hg1820491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565478
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990682
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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