A curated catalogue of human genomic structural variation




Variant Details

Variant: esv991598



Internal ID6727562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:61290960..61309153hg38UCSC Ensembl
Outerchr17:59368321..59386514hg19UCSC Ensembl
Outerchr17:56723103..56741296hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3818194
hg1918194
hg1818194
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565574
SamplesHuRef
Known GenesBCAS3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv991598
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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