A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422205



Internal ID7906302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31516675..32082818hg38UCSC Ensembl
Innerchr15:31808878..32375021hg19UCSC Ensembl
Innerchr15:29596170..30162313hg18UCSC Ensembl
Innerchr15:29596170..30162313hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38566144
hg19566144
hg18566144
hg17566144
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11e196
Supporting Variantsessv5161549
SamplesND01702
Known GenesCHRNA7, OTUD7A
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422205
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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