A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785330



Internal ID19160129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67852181..67914280hg38UCSC Ensembl
Innerchr17:65848297..65910396hg19UCSC Ensembl
Innerchr17:63278759..63340858hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3862100
hg1962100
hg1862100
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893039
Supporting Variants
Samples
Known GenesBPTF
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785330
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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