A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161510



Internal ID8252664
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 StatusS
Merged Variantsesv2422330
Supporting Variants
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)essv5161510
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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