A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890843



Internal ID19185145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42419688..42630633hg38UCSC Ensembl
Outerchr6:42419688..42630633hg38UCSC Ensembl
Innerchr6:42387426..42598371hg19UCSC Ensembl
Outerchr6:42387426..42598371hg19UCSC Ensembl
Innerchr6:42495404..42706349hg18UCSC Ensembl
Outerchr6:42495404..42706349hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38210946
hg19210946
hg18210946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788094
Samples
Known GenesTRERF1, UBR2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890843
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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