A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751115



Internal ID18725361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41573958..41577356hg38UCSC Ensembl
Outerchr15:41573108..41577990hg38UCSC Ensembl
Innerchr15:41866156..41869554hg19UCSC Ensembl
Outerchr15:41865306..41870188hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg384883
hg194883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552368
Supporting Variants
Samples
Known GenesTYRO3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751115
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