A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161450



Internal ID8252727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62506780..63136937hg38UCSC Ensembl
Innerchr7:61897415..62597315hg19UCSC Ensembl
Innerchr7:61534850..62234750hg18UCSC Ensembl
Innerchr7:61341565..62041465hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38630158
hg19699901
hg18699901
hg17699901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422384
Supporting Variants
SamplesND01692
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161450
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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