A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892972



Internal ID19183792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15741192..15754604hg38UCSC Ensembl
Outerchr17:15741192..15754604hg38UCSC Ensembl
Innerchr17:15644506..15657918hg19UCSC Ensembl
Outerchr17:15644506..15657918hg19UCSC Ensembl
Innerchr17:15585231..15598643hg18UCSC Ensembl
Outerchr17:15585231..15598643hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3813413
hg1913413
hg1813413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797122, essv25797635, essv25797390, essv25797968, essv25796510, essv25797245, essv25797872, essv25797453
Samples
Known GenesTBC1D26
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892972
Frequency
Sample Size3017
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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