A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797390



Internal ID19170596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15741192..15754604hg38UCSC Ensembl
Innerchr17:15644506..15657918hg19UCSC Ensembl
Innerchr17:15585231..15598643hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3813413
hg1913413
hg1813413
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892972
Supporting Variants
Samples
Known GenesTBC1D26
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797390
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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