A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006962



Internal ID32665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:46951443..46971306hg38UCSC Ensembl
OuterchrX:46810572..46831782hg19UCSC Ensembl
OuterchrX:46695516..46716726hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3819864
hg1921211
hg1821211
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565437
SamplesHuRef
Known GenesJADE3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006962
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