A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161558



Internal ID7906272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9106517..9214573hg38UCSC Ensembl
Innerchr1:9166576..9274632hg19UCSC Ensembl
Innerchr1:9089163..9197219hg18UCSC Ensembl
Innerchr1:9100842..9208898hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38108057
hg19108057
hg18108057
hg17108057
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422210
Supporting Variants
SamplesND01701
Known GenesGPR157, MIR34A
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161558
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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