A curated catalogue of human genomic structural variation




Variant Details

Variant: esv996568



Internal ID7063610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:28311617..28396650hg38UCSC Ensembl
Outerchr3:28353108..28438141hg19UCSC Ensembl
Outerchr3:28328112..28413145hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3885034
hg1985034
hg1885034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565562
SamplesHuRef
Known GenesAZI2, CMC1, ZCWPW2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv996568
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