A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559359



Internal ID18760435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:134940075..134940634hg38UCSC Ensembl
OuterchrX:134940042..134940699hg38UCSC Ensembl
InnerchrX:134074105..134074664hg19UCSC Ensembl
OuterchrX:134074072..134074729hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758106
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559359
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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