A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546878



Internal ID18747954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:114101972..114102262hg38UCSC Ensembl
Outerchr10:114101909..114102335hg38UCSC Ensembl
Innerchr10:115861731..115862021hg19UCSC Ensembl
Outerchr10:115861668..115862094hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv42e215
Supporting Variantsessv9745625
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546878
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