A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545926



Internal ID18747002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13217452..13218715hg38UCSC Ensembl
Outerchr10:13217181..13218853hg38UCSC Ensembl
Innerchr10:13259452..13260715hg19UCSC Ensembl
Outerchr10:13259181..13260853hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381673
hg191673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744673
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545926
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