A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161557



Internal ID8252829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21023401..21178605hg38UCSC Ensembl
Innerchr3:21064893..21220097hg19UCSC Ensembl
Innerchr3:21039897..21195101hg18UCSC Ensembl
Innerchr3:21039897..21195101hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38155205
hg19155205
hg18155205
hg17155205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422219
Supporting Variants
SamplesND03710
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161557
Frequency
Sample Size181
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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