A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586641



Internal ID7058023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:123817230..123818917hg38UCSC Ensembl
InnerchrX:122951080..122952767hg19UCSC Ensembl
InnerchrX:122778761..122780448hg18UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381688
hg191688
hg181688
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995876
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586641
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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