A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891409



Internal ID19185805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:72123036..72138023hg38UCSC Ensembl
Outerchr8:72123036..72138023hg38UCSC Ensembl
Innerchr8:73035271..73050258hg19UCSC Ensembl
Outerchr8:73035271..73050258hg19UCSC Ensembl
Innerchr8:73197825..73212812hg18UCSC Ensembl
Outerchr8:73197825..73212812hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3814988
hg1914988
hg1814988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786221
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891409
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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