A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891698



Internal ID19186094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102142172..102215271hg38UCSC Ensembl
Outerchr9:102142172..102215271hg38UCSC Ensembl
Innerchr9:104904454..104977553hg19UCSC Ensembl
Outerchr9:104904454..104977553hg19UCSC Ensembl
Innerchr9:103944275..104017374hg18UCSC Ensembl
Outerchr9:103944275..104017374hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3873100
hg1973100
hg1873100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779776, essv25782651
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891698
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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