A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422330



Internal ID8253113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106431831..106701380hg38UCSC Ensembl
Innerchr3:106150678..106420227hg19UCSC Ensembl
Innerchr3:107633368..107902917hg18UCSC Ensembl
Innerchr3:107633368..107902917hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38269550
hg19269550
hg18269550
hg17269550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161510
SamplesND01354
Known Genes
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422330
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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