A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564799



Internal ID7035899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26638360..26650644hg38UCSC Ensembl
Outerchr1:26964851..26977135hg19UCSC Ensembl
Outerchr1:26837438..26849722hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3812285
hg1912285
hg1812285
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994838
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564799
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