A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567616



Internal ID18768692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34251129..34252055hg38UCSC Ensembl
Outerchr6:34251101..34252117hg38UCSC Ensembl
Innerchr6:34218906..34219832hg19UCSC Ensembl
Outerchr6:34218878..34219894hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766363
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567616
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