A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891697



Internal ID19186093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101796603..101882777hg38UCSC Ensembl
Outerchr9:101796603..101882777hg38UCSC Ensembl
Innerchr9:104558885..104645059hg19UCSC Ensembl
Outerchr9:104558885..104645059hg19UCSC Ensembl
Innerchr9:103598706..103684880hg18UCSC Ensembl
Outerchr9:103598706..103684880hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3886175
hg1986175
hg1886175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782284
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891697
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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