A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891494



Internal ID19185890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140028857..140035807hg38UCSC Ensembl
Outerchr8:140028857..140035807hg38UCSC Ensembl
Innerchr8:141038954..141045904hg19UCSC Ensembl
Outerchr8:141038954..141045904hg19UCSC Ensembl
Innerchr8:141108136..141115086hg18UCSC Ensembl
Outerchr8:141108136..141115086hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg386951
hg196951
hg186951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785311
Samples
Known GenesTRAPPC9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891494
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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