A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893828



Internal ID19184648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179338347..179377023hg38UCSC Ensembl
Outerchr3:179338347..179377023hg38UCSC Ensembl
Innerchr3:179056135..179094811hg19UCSC Ensembl
Outerchr3:179056135..179094811hg19UCSC Ensembl
Innerchr3:180538829..180577505hg18UCSC Ensembl
Outerchr3:180538829..180577505hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3838677
hg1938677
hg1838677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783950
Samples
Known GenesMFN1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893828
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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