A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4232288



Internal ID11168140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33113927..33115459hg38UCSC Ensembl
chr3:33155419..33156951hg19UCSC Ensembl
chr3:33130423..33131955hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381533
hg191533
hg181533
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1292944
Supporting Variants
SamplesHuRef
Known GenesCRTAP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4232288
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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