A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010146



Internal ID7074211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:96273501..96291150hg38UCSC Ensembl
Outerchr15:96816730..96834379hg19UCSC Ensembl
Outerchr15:94617734..94635383hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3817650
hg1917650
hg1817650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3563551
SamplesHuRef
Known GenesNR2F2-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010146
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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