A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797877



Internal ID19168627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13384528..13484926hg38UCSC Ensembl
Innerchr17:13287845..13388243hg19UCSC Ensembl
Innerchr17:13228570..13328968hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38100399
hg19100399
hg18100399
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=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797877
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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