A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893829



Internal ID18837963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:179658504..179718510hg38UCSC Ensembl
Outerchr3:179658504..179718510hg38UCSC Ensembl
Innerchr3:179376292..179436298hg19UCSC Ensembl
Outerchr3:179376292..179436298hg19UCSC Ensembl
Innerchr3:180858986..180918992hg18UCSC Ensembl
Outerchr3:180858986..180918992hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3860007
hg1960007
hg1860007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800486
Samples
Known GenesUSP13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893829
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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