A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161238



Internal ID7905952
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 StatusS
Merged Variantsesv2422269
Supporting Variants
SamplesND00727
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)essv5161238
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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