A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994442



Internal ID7079092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:12424569..12441743hg38UCSC Ensembl
Outerchr6:12424801..12441975hg19UCSC Ensembl
Outerchr6:12532787..12549961hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3817175
hg1917175
hg1817175
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564714
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994442
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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