A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893837



Internal ID18837971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:185291669..185483550hg38UCSC Ensembl
Outerchr3:185291669..185483550hg38UCSC Ensembl
Innerchr3:185009457..185201338hg19UCSC Ensembl
Outerchr3:185009457..185201338hg19UCSC Ensembl
Innerchr3:186492151..186684032hg18UCSC Ensembl
Outerchr3:186492151..186684032hg18UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38191882
hg19191882
hg18191882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790252
Samples
Known GenesMAP3K13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893837
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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