A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891268



Internal ID19185664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2029949..2223287hg38UCSC Ensembl
Outerchr8:2029949..2223287hg38UCSC Ensembl
Innerchr8:1978115..2170955hg19UCSC Ensembl
Outerchr8:1978115..2170955hg19UCSC Ensembl
Innerchr8:1965522..2158362hg18UCSC Ensembl
Outerchr8:1965522..2158362hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38193339
hg19192841
hg18192841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787690
Samples
Known GenesMIR7160, MYOM2
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891268
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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