A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890821



Internal ID18838437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31489965..31504943hg38UCSC Ensembl
Outerchr6:31489965..31504943hg38UCSC Ensembl
Innerchr6:31457742..31472720hg19UCSC Ensembl
Outerchr6:31457742..31472720hg19UCSC Ensembl
Innerchr6:31565721..31580699hg18UCSC Ensembl
Outerchr6:31565721..31580699hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3814979
hg1914979
hg1814979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792782
Samples
Known GenesMICB
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890821
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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