A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3558898



Internal ID18413288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:57152068..57212773hg38UCSC Ensembl
OuterchrX:57151781..57213067hg38UCSC Ensembl
InnerchrX:57178501..57239206hg19UCSC Ensembl
OuterchrX:57178214..57239500hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3861287
hg1961287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9757645
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3558898
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