A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3560071



Internal ID18414461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:29184018..29184265hg38UCSC Ensembl
Outerchr1:29183977..29184318hg38UCSC Ensembl
Innerchr1:29510530..29510777hg19UCSC Ensembl
Outerchr1:29510489..29510830hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9758818
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3560071
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