A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558851



Internal ID18759927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:46495938..46497315hg38UCSC Ensembl
OuterchrX:46495854..46497451hg38UCSC Ensembl
InnerchrX:46355373..46356750hg19UCSC Ensembl
OuterchrX:46355289..46356886hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381598
hg191598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757598
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558851
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