A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891420



Internal ID18839130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78710128..78731403hg38UCSC Ensembl
Outerchr8:78710128..78731403hg38UCSC Ensembl
Innerchr8:79622363..79643638hg19UCSC Ensembl
Outerchr8:79622363..79643638hg19UCSC Ensembl
Innerchr8:79784918..79806193hg18UCSC Ensembl
Outerchr8:79784918..79806193hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3821276
hg1921276
hg1821276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797239
Samples
Known GenesLOC101241902, ZC2HC1A
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891420
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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