A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894021



Internal ID18838189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:122306958..122473886hg38UCSC Ensembl
Outerchr4:122306958..122473886hg38UCSC Ensembl
Innerchr4:123228113..123395041hg19UCSC Ensembl
Outerchr4:123228113..123395041hg19UCSC Ensembl
Innerchr4:123447563..123614491hg18UCSC Ensembl
Outerchr4:123447563..123614491hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38166929
hg19166929
hg18166929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784690
Samples
Known GenesADAD1, IL2, KIAA1109
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894021
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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