A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422399



Internal ID7906496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35212221..35291582hg38UCSC Ensembl
Innerchr17:33539240..33618601hg19UCSC Ensembl
Innerchr17:30563353..30642714hg18UCSC Ensembl
Innerchr17:30563353..30642714hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3879362
hg1979362
hg1879362
hg1779362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161457
SamplesND04296
Known GenesSLFN5
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422399
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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