A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567393



Internal ID18768469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21825770..21833984hg38UCSC Ensembl
Outerchr6:21824770..21834769hg38UCSC Ensembl
Innerchr6:21826001..21834215hg19UCSC Ensembl
Outerchr6:21825001..21835000hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9766140
Samples
Known GenesCASC15
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567393
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