A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564169



Internal ID7035269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:47303501..47317337hg38UCSC Ensembl
Outerchr8:48213586..48231454hg19UCSC Ensembl
Outerchr8:48376139..48394007hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3813837
hg1917869
hg1817869
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006968
Supporting Variants
SamplesHuRef
Known GenesSPIDR
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564169
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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