A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542472



Internal ID18743548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135456435..135459123hg38UCSC Ensembl
Outerchr7:135456253..135459450hg38UCSC Ensembl
Innerchr7:135141183..135143871hg19UCSC Ensembl
Outerchr7:135141001..135144198hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg383198
hg193198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741219
Samples
Known GenesCNOT4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542472
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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