A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891328



Internal ID19185724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8662843..8682560hg38UCSC Ensembl
Outerchr8:8662843..8685814hg38UCSC Ensembl
Innerchr8:8520353..8540070hg19UCSC Ensembl
Outerchr8:8520353..8543324hg19UCSC Ensembl
Innerchr8:8557763..8577480hg18UCSC Ensembl
Outerchr8:8557763..8580734hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3822972
hg1922972
hg1822972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780076, essv25787299
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891328
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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