A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890779



Internal ID19185081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:334923..361547hg38UCSC Ensembl
Outerchr6:322474..381918hg38UCSC Ensembl
Innerchr6:334923..361547hg19UCSC Ensembl
Outerchr6:322474..381918hg19UCSC Ensembl
Innerchr6:279923..306547hg18UCSC Ensembl
Outerchr6:267474..326918hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3859445
hg1959445
hg1859445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781927, essv25782172, essv25781783, essv25783109
Samples
Known GenesDUSP22
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890779
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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