A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891249



Internal ID19185645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:361505..380328hg38UCSC Ensembl
Outerchr8:361505..380328hg38UCSC Ensembl
Innerchr8:311505..330328hg19UCSC Ensembl
Outerchr8:311505..330328hg19UCSC Ensembl
Innerchr8:301505..320328hg18UCSC Ensembl
Outerchr8:301505..320328hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3818824
hg1918824
hg1818824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786519
Samples
Known GenesFAM87A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891249
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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