A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785943



Internal ID19173863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:87229758..87267442hg38UCSC Ensembl
Innerchr8:88241986..88279670hg19UCSC Ensembl
Innerchr8:88311102..88348786hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3837685
hg1937685
hg1837685
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891434
Supporting Variants
Samples
Known GenesCNBD1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785943
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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