A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558808



Internal ID18759884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:40645934..40646246hg38UCSC Ensembl
OuterchrX:40645889..40646322hg38UCSC Ensembl
InnerchrX:40505186..40505498hg19UCSC Ensembl
OuterchrX:40505141..40505574hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757555
Samples
Known GenesCXorf38
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558808
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