A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564367



Internal ID7035467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:57374252..57394928hg38UCSC Ensembl
Outerchr12:57768035..57788711hg19UCSC Ensembl
Outerchr12:56054302..56074978hg18UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg3820677
hg1920677
hg1820677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989801
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564367
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer