A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766116



Internal ID18740362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19483344..19495826hg38UCSC Ensembl
Outerchr6:19482809..19496404hg38UCSC Ensembl
Innerchr6:19483575..19496057hg19UCSC Ensembl
Outerchr6:19483040..19496635hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3813596
hg1913596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567369
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766116
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