A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894087



Internal ID19184941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:181738105..182088461hg38UCSC Ensembl
Outerchr4:181738105..182088461hg38UCSC Ensembl
Innerchr4:182659258..183009614hg19UCSC Ensembl
Outerchr4:182659258..183009614hg19UCSC Ensembl
Innerchr4:182896252..183246608hg18UCSC Ensembl
Outerchr4:182896252..183246608hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38350357
hg19350357
hg18350357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791284
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894087
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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