A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161465



Internal ID8252838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89770638..90054875hg38UCSC Ensembl
Innerchr7:89399952..89684189hg19UCSC Ensembl
Innerchr7:89237888..89522125hg18UCSC Ensembl
Innerchr7:89044603..89328840hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38284238
hg19284238
hg18284238
hg17284238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422434
Supporting Variants
SamplesND03792
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161465
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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