A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161296



Internal ID8252840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17126427..17158004hg38UCSC Ensembl
Innerchr1:17452922..17484499hg19UCSC Ensembl
Innerchr1:17325509..17357086hg18UCSC Ensembl
Innerchr1:17198228..17229805hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3831578
hg1931578
hg1831578
hg1731578
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422211
Supporting Variants
SamplesND03833
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161296
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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