A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891418



Internal ID19185814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77639466..77721032hg38UCSC Ensembl
Outerchr8:77639466..77734645hg38UCSC Ensembl
Innerchr8:78551702..78633267hg19UCSC Ensembl
Outerchr8:78551702..78646880hg19UCSC Ensembl
Innerchr8:78714257..78795822hg18UCSC Ensembl
Outerchr8:78714257..78809435hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3895180
hg1995179
hg1895179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799645, essv25801053, essv25783271
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891418
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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