A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790813



Internal ID19171271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103317288..103361793hg38UCSC Ensembl
Innerchr9:106079570..106124075hg19UCSC Ensembl
Innerchr9:105119391..105163896hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3844506
hg1944506
hg1844506
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891702
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790813
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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