A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891702



Internal ID19186098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103317288..103361793hg38UCSC Ensembl
Outerchr9:103317288..103361793hg38UCSC Ensembl
Innerchr9:106079570..106124075hg19UCSC Ensembl
Outerchr9:106079570..106124075hg19UCSC Ensembl
Innerchr9:105119391..105163896hg18UCSC Ensembl
Outerchr9:105119391..105163896hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3844506
hg1944506
hg1844506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790813
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891702
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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