A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161525



Internal ID8252842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135342736..135437765hg38UCSC Ensembl
Innerchr9:138234582..138329611hg19UCSC Ensembl
Innerchr9:137374403..137469432hg18UCSC Ensembl
Innerchr9:135460527..135555556hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3895030
hg1995030
hg1895030
hg1795030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422430
Supporting Variants
SamplesND03834
Known GenesC9orf62
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161525
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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