A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161479



Internal ID7906193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133271664..133450541hg38UCSC Ensembl
Innerchr10:135085168..135264045hg19UCSC Ensembl
Innerchr10:134935158..135114035hg18UCSC Ensembl
Innerchr10:134974049..135152926hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38178878
hg19178878
hg18178878
hg17178878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422352
Supporting Variants
SamplesND03123
Known GenesADAM8, CALY, ECHS1, FUOM, MIR3944, MTG1, PAOX, PRAP1, SPRN, TUBGCP2, ZNF511
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161479
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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