A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892989



Internal ID19183809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27663007..27756365hg38UCSC Ensembl
Outerchr17:27663007..27756365hg38UCSC Ensembl
Innerchr17:25990033..26083391hg19UCSC Ensembl
Outerchr17:25990033..26083391hg19UCSC Ensembl
Innerchr17:23014160..23107518hg18UCSC Ensembl
Outerchr17:23014160..23107518hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3893359
hg1993359
hg1893359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787863
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892989
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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