A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739655



Internal ID18713901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168316569..168317898hg38UCSC Ensembl
Outerchr6:168316285..168318111hg38UCSC Ensembl
Innerchr6:168717249..168718578hg19UCSC Ensembl
Outerchr6:168716965..168718791hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381827
hg191827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540908
Supporting Variants
Samples
Known GenesDACT2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739655
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