A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564661



Internal ID7035761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:69960754..69976928hg38UCSC Ensembl
Outerchr8:70872989..70889163hg19UCSC Ensembl
Outerchr8:71035543..71051717hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3816175
hg1916175
hg1816175
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000906
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564661
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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