A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5161389



Internal ID7906103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75195128..75546782hg38UCSC Ensembl
Innerchr3:75244279..75595933hg19UCSC Ensembl
Innerchr3:75326969..75678623hg18UCSC Ensembl
Innerchr3:75326969..75678623hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38351655
hg19351655
hg18351655
hg17351655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2422240
Supporting Variants
SamplesND01708
Known GenesFAM86DP, MIR4444-1
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)essv5161389
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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