A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893851



Internal ID19184671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195833068..195929860hg38UCSC Ensembl
Outerchr3:195833068..195929860hg38UCSC Ensembl
Innerchr3:195559939..195656731hg19UCSC Ensembl
Outerchr3:195559939..195656731hg19UCSC Ensembl
Innerchr3:197044336..197141128hg18UCSC Ensembl
Outerchr3:197044336..197141128hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3896793
hg1996793
hg1896793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785561
Samples
Known GenesMIR6829, TNK2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893851
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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