A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161242



Internal ID8252806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134718355..135024828hg38UCSC Ensembl
Innerchr4:135639510..135945983hg19UCSC Ensembl
Innerchr4:135858960..136165433hg18UCSC Ensembl
Innerchr4:135997115..136303588hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38306474
hg19306474
hg18306474
hg17306474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422408
Supporting Variants
SamplesND03627
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161242
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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