A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760855



Internal ID18388415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:77293459..77294207hg38UCSC Ensembl
Outerchr3:77293350..77294404hg38UCSC Ensembl
Innerchr3:77342610..77343358hg19UCSC Ensembl
Outerchr3:77342501..77343555hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381055
hg191055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562108
Supporting Variants
Samples
Known GenesROBO2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760855
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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