A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763482



Internal ID18737728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141709003..141709055hg38UCSC Ensembl
chr4:142630156..142630208hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564735
Supporting Variants
Samples
Known GenesIL15
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763482
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