A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000574



Internal ID7065704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75205229..75224130hg38UCSC Ensembl
Outerchr16:75239127..75258028hg19UCSC Ensembl
Outerchr16:73796628..73815529hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3818902
hg1918902
hg1818902
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564835
SamplesHuRef
Known GenesCTRB1, CTRB2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000574
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