A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890780



Internal ID19185082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:296257..361547hg38UCSC Ensembl
Outerchr6:274847..381918hg38UCSC Ensembl
Innerchr6:296257..361547hg19UCSC Ensembl
Outerchr6:274847..381918hg19UCSC Ensembl
Innerchr6:241257..306547hg18UCSC Ensembl
Outerchr6:219847..326918hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38107072
hg19107072
hg18107072
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788952, essv25786449, essv25801679
Samples
Known GenesDUSP22
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890780
Frequency
Sample Size3017
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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