A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891434



Internal ID19185830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:87229758..87267442hg38UCSC Ensembl
Outerchr8:87229758..87267442hg38UCSC Ensembl
Innerchr8:88241986..88279670hg19UCSC Ensembl
Outerchr8:88241986..88279670hg19UCSC Ensembl
Innerchr8:88311102..88348786hg18UCSC Ensembl
Outerchr8:88311102..88348786hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3837685
hg1937685
hg1837685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785943, essv25784637
Samples
Known GenesCNBD1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891434
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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