A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161527



Internal ID8252752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44548713..44762236hg38UCSC Ensembl
Innerchr10:45044161..45257684hg19UCSC Ensembl
Innerchr10:44364167..44577690hg18UCSC Ensembl
Innerchr10:44364167..44577690hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38213524
hg19213524
hg18213524
hg17213524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422287
Supporting Variants
SamplesND01757
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161527
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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