A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891332



Internal ID18839042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9263888..9327636hg38UCSC Ensembl
Outerchr8:9263888..9327636hg38UCSC Ensembl
Innerchr8:9121398..9185146hg19UCSC Ensembl
Outerchr8:9121398..9185146hg19UCSC Ensembl
Innerchr8:9158808..9222556hg18UCSC Ensembl
Outerchr8:9158808..9222556hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3863749
hg1963749
hg1863749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800671
Samples
Known GenesLOC157273
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891332
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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