A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891307



Internal ID19185703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6236885..6313803hg38UCSC Ensembl
Outerchr8:6206048..6342924hg38UCSC Ensembl
Innerchr8:6094406..6171324hg19UCSC Ensembl
Outerchr8:6063569..6200445hg19UCSC Ensembl
Innerchr8:6081814..6158732hg18UCSC Ensembl
Outerchr8:6050977..6187853hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38136877
hg19136877
hg18136877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796280, essv25784441, essv25796267, essv25798280, essv25784792, essv25784919, essv25783462, essv25778318, essv25784651
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891307
Frequency
Sample Size3017
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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