A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797886



Internal ID19177082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13384528..13488405hg38UCSC Ensembl
Innerchr17:13287845..13391722hg19UCSC Ensembl
Innerchr17:13228570..13332447hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38103878
hg19103878
hg18103878
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892960
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797886
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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