A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894068



Internal ID19184922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167283413..167343097hg38UCSC Ensembl
Outerchr4:167283413..167343098hg38UCSC Ensembl
Innerchr4:168204564..168264248hg19UCSC Ensembl
Outerchr4:168204564..168264249hg19UCSC Ensembl
Innerchr4:168441139..168500823hg18UCSC Ensembl
Outerchr4:168441139..168500824hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3859686
hg1959686
hg1859686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788052, essv25793000, essv25788708
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894068
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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