A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761772



Internal ID18389332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186071719..186072001hg38UCSC Ensembl
Outerchr3:186071660..186072114hg38UCSC Ensembl
Innerchr3:185789508..185789790hg19UCSC Ensembl
Outerchr3:185789449..185789903hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563025
Supporting Variants
Samples
Known GenesETV5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761772
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