A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891472



Internal ID18839182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119104995..119171411hg38UCSC Ensembl
Outerchr8:119104995..119171411hg38UCSC Ensembl
Innerchr8:120117234..120183650hg19UCSC Ensembl
Outerchr8:120117234..120183650hg19UCSC Ensembl
Innerchr8:120186415..120252831hg18UCSC Ensembl
Outerchr8:120186415..120252831hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3866417
hg1966417
hg1866417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801109
Samples
Known GenesCOLEC10
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891472
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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