A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894072



Internal ID18838240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:176316166..176329340hg38UCSC Ensembl
Outerchr4:176311557..176329340hg38UCSC Ensembl
Innerchr4:177237317..177250491hg19UCSC Ensembl
Outerchr4:177232708..177250491hg19UCSC Ensembl
Innerchr4:177474311..177487485hg18UCSC Ensembl
Outerchr4:177469702..177487485hg18UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg3817784
hg1917784
hg1817784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801041, essv25801035
Samples
Known GenesSPCS3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894072
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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