A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758129



Internal ID18732375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:138477440..138477658hg38UCSC Ensembl
OuterchrX:138477405..138477659hg38UCSC Ensembl
InnerchrX:137559598..137559816hg19UCSC Ensembl
OuterchrX:137559563..137559817hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758129
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