A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894091



Internal ID19184945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186772422..187027471hg38UCSC Ensembl
Outerchr4:186772422..187027471hg38UCSC Ensembl
Innerchr4:187693576..187948625hg19UCSC Ensembl
Outerchr4:187693576..187948625hg19UCSC Ensembl
Innerchr4:187930570..188185619hg18UCSC Ensembl
Outerchr4:187930570..188185619hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38255050
hg19255050
hg18255050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790690
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894091
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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