A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799315



Internal ID18827253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:60812316..60844613hg38UCSC Ensembl
Innerchr17:58889677..58921974hg19UCSC Ensembl
Innerchr17:56244459..56276756hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3832298
hg1932298
hg1832298
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893034
Supporting Variants
Samples
Known GenesBCAS3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799315
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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