A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9741219



Internal ID18715465
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 StatusS
Merged Variantsesv3542472
Supporting Variants
Samples
Known GenesCNOT4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9741219
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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