A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv394e215



Internal ID22785904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71861682..71862083hg38UCSC Ensembl
chr6:72571385..72571786hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3539954, esv3539955
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)dgv394e215
Frequency
Sample Size767
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer