A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161488



Internal ID7906202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32506737..32929014hg38UCSC Ensembl
Innerchr15:32798938..33221215hg19UCSC Ensembl
Innerchr15:30586230..31008507hg18UCSC Ensembl
Innerchr15:30586230..31008507hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38422278
hg19422278
hg18422278
hg17422278
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422296
Supporting Variants
SamplesND05461
Known GenesARHGAP11A, FMN1, GOLGA8R, GREM1, LOC100131315, LOC100996255, SCG5, WHAMMP1
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161488
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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