A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893813



Internal ID19184633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168634072..168719722hg38UCSC Ensembl
Outerchr3:168634072..168719722hg38UCSC Ensembl
Innerchr3:168351860..168437510hg19UCSC Ensembl
Outerchr3:168351860..168437510hg19UCSC Ensembl
Innerchr3:169834554..169920204hg18UCSC Ensembl
Outerchr3:169834554..169920204hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3885651
hg1985651
hg1885651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784590
Samples
Known GenesEGFEM1P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893813
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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