A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1002540



Internal ID6714675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:65438105..65443768hg38UCSC Ensembl
InnerchrX:64657985..64663648hg19UCSC Ensembl
InnerchrX:64574710..64580373hg18UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg385664
hg195664
hg185664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586491
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1002540
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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