A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766429



Internal ID18740675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:39337540..39339729hg38UCSC Ensembl
Outerchr6:39337519..39339769hg38UCSC Ensembl
Innerchr6:39305316..39307505hg19UCSC Ensembl
Outerchr6:39305295..39307545hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382251
hg192251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567682
Supporting Variants
Samples
Known GenesKIF6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766429
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