A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787886



Internal ID19177809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:66756824..66797065hg38UCSC Ensembl
Innerchr1:67222507..67262748hg19UCSC Ensembl
Innerchr1:66995095..67035336hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3840242
hg1940242
hg1840242
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893623
Supporting Variants
Samples
Known GenesTCTEX1D1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787886
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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