A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893038



Internal ID19183858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67852181..67875443hg38UCSC Ensembl
Outerchr17:67852181..67875443hg38UCSC Ensembl
Innerchr17:65848297..65871559hg19UCSC Ensembl
Outerchr17:65848297..65871559hg19UCSC Ensembl
Innerchr17:63278759..63302021hg18UCSC Ensembl
Outerchr17:63278759..63302021hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3823263
hg1923263
hg1823263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781696
Samples
Known GenesBPTF
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893038
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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