A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891443



Internal ID19185839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95089558..95097142hg38UCSC Ensembl
Outerchr8:95089558..95097142hg38UCSC Ensembl
Innerchr8:96101786..96109370hg19UCSC Ensembl
Outerchr8:96101786..96109370hg19UCSC Ensembl
Innerchr8:96170962..96178546hg18UCSC Ensembl
Outerchr8:96170962..96178546hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg387585
hg197585
hg187585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785368
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891443
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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