A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893838



Internal ID19184658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186374785..186477534hg38UCSC Ensembl
Outerchr3:186374785..186477534hg38UCSC Ensembl
Innerchr3:186092574..186195323hg19UCSC Ensembl
Outerchr3:186092574..186195323hg19UCSC Ensembl
Innerchr3:187575268..187678017hg18UCSC Ensembl
Outerchr3:187575268..187678017hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38102750
hg19102750
hg18102750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792553
Samples
Known GenesLOC253573
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893838
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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